A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696491



Internal ID15433143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:60647292..60663319hg38UCSC Ensembl
Innerchr4:61513010..61529037hg19UCSC Ensembl
Innerchr4:61195605..61211632hg18UCSC Ensembl
Innerchr4:61341776..61357803hg17UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3816028
hg1916028
hg1816028
hg1716028
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519020
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696491
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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