A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3625050



Internal ID18923331
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:43184487..43211021hg38UCSC Ensembl
Innerchr4:43186504..43213038hg19UCSC Ensembl
Innerchr4:42881261..42907795hg18UCSC Ensembl
Cytoband4p13
Allele length
AssemblyAllele length
hg3826535
hg1926535
hg1826535
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004634
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)nssv3625050
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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