A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704349



Internal ID15094315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:31809755..31977216hg38UCSC Ensembl
InnerchrX:31827872..31995333hg19UCSC Ensembl
InnerchrX:31737793..31905254hg18UCSC Ensembl
InnerchrX:31587529..31754990hg17UCSC Ensembl
CytobandXp21.1
Allele length
AssemblyAllele length
hg38167462
hg19167462
hg18167462
hg17167462
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527851
Supporting Variants
Samples
Known GenesDMD
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704349
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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