A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3625052



Internal ID18923333
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43628242..43674291hg38UCSC Ensembl
Innerchr4:43630259..43676308hg19UCSC Ensembl
Innerchr4:43325016..43371065hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3846050
hg1946050
hg1846050
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1010430
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)nssv3625052
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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