A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3641192



Internal ID18939473
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:142866890..142879808hg38UCSC Ensembl
Innerchr4:143788043..143800961hg19UCSC Ensembl
Innerchr4:144007493..144020411hg18UCSC Ensembl
Cytoband4q31.21
Allele length
AssemblyAllele length
hg3812919
hg1912919
hg1812919
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033772
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)nssv3641192
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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