A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699640



Internal ID15436292
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5727017..5732564hg38UCSC Ensembl
Innerchr6:5727250..5732797hg19UCSC Ensembl
Innerchr6:5672249..5677796hg18UCSC Ensembl
Innerchr6:5672249..5677796hg17UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg385548
hg195548
hg185548
hg175548
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523810
Supporting Variants
Samples
Known GenesFARS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699640
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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