A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv680980



Internal ID15070946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:965228..1008903hg38UCSC Ensembl
Innerchr3:1006912..1050587hg19UCSC Ensembl
Innerchr3:981912..1025587hg18UCSC Ensembl
Innerchr3:981912..1025587hg17UCSC Ensembl
Cytoband3p26.3
Allele length
AssemblyAllele length
hg3843676
hg1943676
hg1843676
hg1743676
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517343
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv680980
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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