A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525444



Internal ID18823725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:87183164..87488715hg38UCSC Ensembl
Innerchr13:87835419..88140970hg19UCSC Ensembl
Innerchr13:86633420..86938971hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg38305552
hg19305552
hg18305552
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1043448
Supporting Variants
Samples
Known GenesMIR4500HG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3525444
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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