A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1042985



Internal ID19132204
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:91455590..91480444hg38UCSC Ensembl
Innerchr13:92107844..92132698hg19UCSC Ensembl
Innerchr13:90905845..90930699hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3824855
hg1924855
hg1824855
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3713273
Samples
Known GenesGPC5
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1042985
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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