A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698487



Internal ID15435139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:5727017..5736889hg38UCSC Ensembl
Innerchr6:5727250..5737122hg19UCSC Ensembl
Innerchr6:5672249..5682121hg18UCSC Ensembl
Innerchr6:5672249..5682121hg17UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg389873
hg199873
hg189873
hg179873
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522836
Supporting Variants
Samples
Known GenesFARS2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698487
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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