A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv696956



Internal ID15433608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:44276139..44280207hg38UCSC Ensembl
Innerchr22:44672019..44676087hg19UCSC Ensembl
Innerchr22:43003352..43007420hg18UCSC Ensembl
Innerchr22:42996920..43000988hg17UCSC Ensembl
Cytoband22q13.31
Allele length
AssemblyAllele length
hg384069
hg194069
hg184069
hg174069
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519623
Supporting Variants
Samples
Known GenesKIAA1644
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv696956
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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