A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv519786



Internal ID15100393
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:85649751..85907957hg38UCSC Ensembl
InnerchrX:84904756..85162962hg19UCSC Ensembl
InnerchrX:84791412..85049618hg18UCSC Ensembl
InnerchrX:84710901..84969107hg17UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg38258207
hg19258207
hg18258207
hg17258207
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv671840, nssv703256, nssv658617, nssv696662
Samples
Known GenesCHM
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv519786
Frequency
Sample Size2026
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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