A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv653586



Internal ID15390238
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:147039600..147050756hg38UCSC Ensembl
InnerchrX:146121118..146132274hg19UCSC Ensembl
InnerchrX:145928810..145939966hg18UCSC Ensembl
InnerchrX:145826664..145837820hg17UCSC Ensembl
CytobandXq27.3
Allele length
AssemblyAllele length
hg3811157
hg1911157
hg1811157
hg1711157
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517085
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv653586
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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