A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525485



Internal ID18823766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:91842839..91867234hg38UCSC Ensembl
Innerchr13:92495093..92519488hg19UCSC Ensembl
Innerchr13:91293094..91317489hg18UCSC Ensembl
Cytoband13q31.3
Allele length
AssemblyAllele length
hg3824396
hg1924396
hg1824396
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1041361
Supporting Variants
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)nssv3525485
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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