A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042019



Internal ID19131238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63688137..63799095hg38UCSC Ensembl
Innerchr13:64262270..64373228hg19UCSC Ensembl
Innerchr13:63160271..63271229hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38110959
hg19110959
hg18110959
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1686n100
Supporting Variantsnssv3526635, nssv3526636, nssv3526648, nssv3526641, nssv3526631, nssv3711783, nssv3526634, nssv3526646, nssv3526639, nssv3711782, nssv3526645, nssv3526632, nssv3526643, nssv3526629, nssv3526628, nssv3526642, nssv3526637, nssv3711781, nssv3526638, nssv3526644, nssv3711779, nssv3526630, nssv3526640, nssv3526633, nssv3711780, nssv3526647
Samples
Known GenesLINC00395, OR7E156P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042019
Frequency
Sample Size11257
Observed Gain0
Observed Loss26
Observed Complex0
Frequencyn/a


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