A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv528655



Internal ID15455948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:69051331..69103917hg38UCSC Ensembl
InnerchrX:68271174..68323760hg19UCSC Ensembl
InnerchrX:68187899..68240485hg18UCSC Ensembl
InnerchrX:68054195..68106781hg17UCSC Ensembl
CytobandXq13.1
Allele length
AssemblyAllele length
hg3852587
hg1952587
hg1852587
hg1752587
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv705289
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv528655
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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