A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697301



Internal ID15433953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:125363140..125470882hg38UCSC Ensembl
InnerchrX:124496989..124604731hg19UCSC Ensembl
InnerchrX:124324670..124432412hg18UCSC Ensembl
InnerchrX:124222524..124330266hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38107743
hg19107743
hg18107743
hg17107743
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520238
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697301
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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