A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3625002



Internal ID18923283
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:35369560..35409909hg38UCSC Ensembl
Innerchr4:35371182..35411531hg19UCSC Ensembl
Innerchr4:35047577..35087926hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3840350
hg1940350
hg1840350
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1005307
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)nssv3625002
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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