A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519305



Internal ID15099912
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:48235711..48294993hg38UCSC Ensembl
InnerchrX:48095146..48154428hg19UCSC Ensembl
InnerchrX:47980090..48039372hg18UCSC Ensembl
InnerchrX:47851400..47910682hg17UCSC Ensembl
CytobandXp11.23
Allele length
AssemblyAllele length
hg3859283
hg1959283
hg1859283
hg1759283
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv696778
Samples
Known GenesSSX1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519305
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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