A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1051276



Internal ID19140495
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:94093741..94220240hg38UCSC Ensembl
Innerchr13:94745995..94872494hg19UCSC Ensembl
Innerchr13:93543996..93670495hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg38126500
hg19126500
hg18126500
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713277
Samples
Known GenesGPC6, GPC6-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1051276
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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