A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527359



Internal ID15454652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:28281933..28287196hg38UCSC Ensembl
InnerchrX:28300050..28305313hg19UCSC Ensembl
InnerchrX:28209971..28215234hg18UCSC Ensembl
InnerchrX:28059707..28064970hg17UCSC Ensembl
CytobandXp21.3
Allele length
AssemblyAllele length
hg385264
hg195264
hg185264
hg175264
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703789
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527359
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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