A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1056944



Internal ID19146163
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:64041842..64080299hg38UCSC Ensembl
Innerchr16:64075746..64114203hg19UCSC Ensembl
Innerchr16:62633247..62671704hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3838458
hg1938458
hg1838458
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2993n100
Supporting Variantsnssv3559412, nssv3559391, nssv3559392, nssv3559408, nssv3559404, nssv3559396, nssv3559414, nssv3559416, nssv3559399, nssv3559407, nssv3559401, nssv3559405, nssv3559402, nssv3559390, nssv3559413, nssv3559393, nssv3559409, nssv3559394, nssv3559406, nssv3559411, nssv3559397, nssv3559398, nssv3559410, nssv3559395, nssv3559400, nssv3559389, nssv3559415, nssv3559403
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1056944
Frequency
Sample Size11257
Observed Gain0
Observed Loss28
Observed Complex0
Frequencyn/a


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