A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682832



Internal ID15419484
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:125608357..125906451hg38UCSC Ensembl
InnerchrX:124742354..125040433hg19UCSC Ensembl
InnerchrX:124570035..124868114hg18UCSC Ensembl
InnerchrX:124467889..124765968hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38298095
hg19298080
hg18298080
hg17298080
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517568
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682832
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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