A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1038263



Internal ID19127482
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63727459..63831177hg38UCSC Ensembl
Innerchr13:64301592..64405310hg19UCSC Ensembl
Innerchr13:63199593..63303311hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38103719
hg19103719
hg18103719
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1689n100
Supporting Variantsnssv3526693, nssv3526688, nssv3526692, nssv3526683, nssv3711791, nssv3526687, nssv3526691, nssv3526682, nssv3526695, nssv3526697, nssv3526686, nssv3526698, nssv3526685, nssv3711793, nssv3526694, nssv3526699, nssv3526689, nssv3526696, nssv3711790, nssv3526690, nssv3711792, nssv3526684
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)nsv1038263
Frequency
Sample Size11257
Observed Gain12
Observed Loss10
Observed Complex0
Frequencyn/a


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