A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047128



Internal ID19136347
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:63673517..63788003hg38UCSC Ensembl
Innerchr13:64247650..64362136hg19UCSC Ensembl
Innerchr13:63145651..63260137hg18UCSC Ensembl
Cytoband13q21.31
Allele length
AssemblyAllele length
hg38114487
hg19114487
hg18114487
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1686n100
Supporting Variantsnssv3526613
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)nsv1047128
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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