A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1035144



Internal ID19124363
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:93630791..93699921hg38UCSC Ensembl
Innerchr13:94283044..94352174hg19UCSC Ensembl
Innerchr13:93081045..93150175hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3869131
hg1969131
hg1869131
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3525493
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)nsv1035144
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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