A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3724889



Internal ID19023170
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:43421138..43450763hg38UCSC Ensembl
Innerchr19:43925290..43954915hg19UCSC Ensembl
Innerchr19:48617130..48646755hg18UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg3829626
hg1929626
hg1829626
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1061862
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3724889
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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