A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv697724



Internal ID15434376
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:131759929..131834263hg38UCSC Ensembl
InnerchrX:130893957..130968291hg19UCSC Ensembl
InnerchrX:130721638..130795972hg18UCSC Ensembl
InnerchrX:130619492..130693826hg17UCSC Ensembl
CytobandXq26.2
Allele length
AssemblyAllele length
hg3874335
hg1974335
hg1874335
hg1774335
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520989
Supporting Variants
Samples
Known GenesLOC286467
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv697724
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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