A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527647



Internal ID15454940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:117118541..117243229hg38UCSC Ensembl
InnerchrX:116252509..116377192hg19UCSC Ensembl
InnerchrX:116136537..116261220hg18UCSC Ensembl
InnerchrX:116034391..116159074hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38124689
hg19124684
hg18124684
hg17124684
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv704118
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527647
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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