A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv602160



Internal ID16389569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:32487705..32524531hg38UCSC Ensembl
Innerchr6:32455482..32492308hg19UCSC Ensembl
Innerchr6:32563460..32600286hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3836827
hg1936827
hg1836827
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv10501n54
Supporting Variantsnssv1054423, nssv1054385, nssv1054395, nssv1054416, nssv1054418, nssv1054382, nssv1054401, nssv1054372, nssv1054377, nssv1054396, nssv1054410, nssv1054414, nssv1054399, nssv1054407, nssv1054406, nssv1054392, nssv1054389, nssv1054403, nssv1054421, nssv1054397, nssv1054387, nssv1054419, nssv1054378, nssv1054400, nssv1054409, nssv1054379, nssv1054374, nssv1054381, nssv1054383, nssv1054408, nssv1054376, nssv1054405, nssv1054413, nssv1054393, nssv1054422, nssv1054411, nssv1054390, nssv1054398, nssv1054380, nssv1054375, nssv1054417, nssv1054412, nssv1054394, nssv1054402, nssv1054373, nssv1054415, nssv1054420, nssv1054371, nssv1054388, nssv1054391, nssv1054384, nssv1054386, nssv1054404
Samples
Known GenesHLA-DRB5
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv602160
Frequency
Sample Size17421
Observed Gain0
Observed Loss53
Observed Complex0
Frequencyn/a


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