A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv605099



Internal ID16045822
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:162164009..162165759hg38UCSC Ensembl
Innerchr6:162585041..162586791hg19UCSC Ensembl
Innerchr6:162505031..162506781hg18UCSC Ensembl
Cytoband6q26
Allele length
AssemblyAllele length
hg381751
hg191751
hg181751
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11007n54
Supporting Variantsnssv1075461, nssv1075471, nssv1075464, nssv1075482, nssv1075481, nssv1075473, nssv1075489, nssv1075467, nssv1075486, nssv1075465, nssv1075485, nssv1075480, nssv1075487, nssv1075469, nssv1075476, nssv1075458, nssv1075470, nssv1075468, nssv1075478, nssv1075463, nssv1075466, nssv1075475, nssv1075474, nssv1075460, nssv1075483, nssv1075488, nssv1075479, nssv1075459, nssv1075484, nssv1075477, nssv1075462, nssv1075472, nssv1075490, nssv1075491
Samples
Known GenesPARK2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv605099
Frequency
Sample Size17421
Observed Gain0
Observed Loss34
Observed Complex0
Frequencyn/a


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