A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697152



Internal ID15433804
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:116990070..116994073hg38UCSC Ensembl
InnerchrX:116124038..116128041hg19UCSC Ensembl
InnerchrX:116008066..116012069hg18UCSC Ensembl
InnerchrX:115905920..115909923hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg384004
hg194004
hg184004
hg174004
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519966
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697152
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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