A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701645



Internal ID15438297
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:46313984..46326503hg38UCSC Ensembl
Innerchr22:46709881..46722400hg19UCSC Ensembl
Innerchr22:45088545..45101064hg18UCSC Ensembl
Innerchr22:45030400..45042919hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg3812520
hg1912520
hg1812520
hg1712520
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525512
Supporting Variants
Samples
Known GenesGTSE1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701645
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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