A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3620695



Internal ID18918976
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:34768672..34817577hg38UCSC Ensembl
Innerchr4:34770294..34819199hg19UCSC Ensembl
Innerchr4:34446689..34495594hg18UCSC Ensembl
Cytoband4p15.1
Allele length
AssemblyAllele length
hg3848906
hg1948906
hg1848906
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004107
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)nssv3620695
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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