A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698652



Internal ID15435304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:87041530..87049758hg38UCSC Ensembl
InnerchrX:86296533..86304761hg19UCSC Ensembl
InnerchrX:86183189..86191417hg18UCSC Ensembl
InnerchrX:86102678..86110906hg17UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg388229
hg198229
hg188229
hg178229
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv522982
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698652
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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