A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv687917



Internal ID15424569
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:62709286..62929219hg38UCSC Ensembl
InnerchrX:61928756..62148689hg19UCSC Ensembl
InnerchrX:61845481..62065414hg18UCSC Ensembl
InnerchrX:61711777..61931710hg17UCSC Ensembl
CytobandXq11.1
Allele length
AssemblyAllele length
hg38219934
hg19219934
hg18219934
hg17219934
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv520427
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv687917
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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