A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697295



Internal ID15433947
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:31592958..31901542hg38UCSC Ensembl
InnerchrX:31611075..31919659hg19UCSC Ensembl
InnerchrX:31520996..31829580hg18UCSC Ensembl
InnerchrX:31370732..31679316hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38308585
hg19308585
hg18308585
hg17308585
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520230
Supporting Variants
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697295
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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