A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv704490



Internal ID15441142
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:22957684..22992008hg38UCSC Ensembl
InnerchrX:22975801..23010125hg19UCSC Ensembl
InnerchrX:22885722..22920046hg18UCSC Ensembl
InnerchrX:22735458..22769782hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3834325
hg1934325
hg1834325
hg1734325
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv527975
Supporting Variants
Samples
Known GenesLOC100873065
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv704490
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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