A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527982



Internal ID15455275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:23252810..23281291hg38UCSC Ensembl
InnerchrX:23270927..23299408hg19UCSC Ensembl
InnerchrX:23180848..23209329hg18UCSC Ensembl
InnerchrX:23030584..23059065hg17UCSC Ensembl
CytobandXp22.11
Allele length
AssemblyAllele length
hg3828482
hg1928482
hg1828482
hg1728482
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704501
Samples
Known GenesLOC100873065
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527982
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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