A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683846



Internal ID15420498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:106077891..106105879hg38UCSC Ensembl
Innerchr7:105718337..105746325hg19UCSC Ensembl
Innerchr7:105505573..105533561hg18UCSC Ensembl
Innerchr7:105312288..105340276hg17UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg3827989
hg1927989
hg1827989
hg1727989
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520366
Supporting Variants
Samples
Known GenesSYPL1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683846
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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