A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3525449



Internal ID18823730
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:87547782..87623509hg38UCSC Ensembl
Innerchr13:88200037..88275764hg19UCSC Ensembl
Innerchr13:86998038..87073765hg18UCSC Ensembl
Cytoband13q31.2
Allele length
AssemblyAllele length
hg3875728
hg1975728
hg1875728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1048269
Supporting Variants
Samples
Known GenesMIR4500, MIR4500HG
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3525449
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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