A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1050202



Internal ID19139421
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:93309225..93330135hg38UCSC Ensembl
Innerchr13:93961478..93982388hg19UCSC Ensembl
Innerchr13:92759479..92780389hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3820911
hg1920911
hg1820911
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525490
Samples
Known GenesGPC6
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1050202
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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