A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv672849



Internal ID15409501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr5:104365978..104452850hg38UCSC Ensembl
Innerchr5:103701679..103788551hg19UCSC Ensembl
Innerchr5:103729578..103816450hg18UCSC Ensembl
Innerchr5:103729578..103816450hg17UCSC Ensembl
Cytoband5q21.2
Allele length
AssemblyAllele length
hg3886873
hg1986873
hg1886873
hg1786873
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519706
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv672849
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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