A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv678650



Internal ID15415302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:10062378..10069501hg38UCSC Ensembl
Innerchr6:10062611..10069734hg19UCSC Ensembl
Innerchr6:10170597..10177720hg18UCSC Ensembl
Innerchr6:10170597..10177720hg17UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg387124
hg197124
hg187124
hg177124
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516522
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv678650
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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