A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv698838



Internal ID15435490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:143585329..143604454hg38UCSC Ensembl
InnerchrX:142673154..142692263hg19UCSC Ensembl
InnerchrX:142500820..142519929hg18UCSC Ensembl
InnerchrX:142398674..142417783hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3819126
hg1919110
hg1819110
hg1719110
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv523133
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv698838
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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