A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3625141



Internal ID18923422
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:49032908..49063952hg38UCSC Ensembl
Innerchr4:49034925..49065969hg19UCSC Ensembl
Innerchr4:48729682..48760726hg18UCSC Ensembl
Cytoband4p11
Allele length
AssemblyAllele length
hg3831045
hg1931045
hg1831045
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1006591
Supporting Variants
Samples
Known GenesCWH43
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3625141
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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