A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3632596



Internal ID18930877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:107297865..107469342hg38UCSC Ensembl
Innerchr4:108219022..108390499hg19UCSC Ensembl
Innerchr4:108438471..108609948hg18UCSC Ensembl
Cytoband4q25
Allele length
AssemblyAllele length
hg38171478
hg19171478
hg18171478
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1012810
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)nssv3632596
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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