A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037962



Internal ID19127181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63680711..63796662hg38UCSC Ensembl
Innerchr13:64254844..64370795hg19UCSC Ensembl
Innerchr13:63152845..63268796hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38115952
hg19115952
hg18115952
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1686n100
Supporting Variantsnssv3526615, nssv3526614
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)nsv1037962
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer