A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697556



Internal ID15087522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr22:35410822..35412774hg38UCSC Ensembl
Innerchr22:35806815..35808767hg19UCSC Ensembl
Innerchr22:34136815..34138767hg18UCSC Ensembl
Innerchr22:34131369..34133321hg17UCSC Ensembl
Cytoband22q12.3
Allele length
AssemblyAllele length
hg381953
hg191953
hg181953
hg171953
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520686
Supporting Variants
Samples
Known GenesMCM5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697556
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer