A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515695



Internal ID15443306
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:113047245..113183439hg38UCSC Ensembl
InnerchrX:112290473..112426666hg19UCSC Ensembl
InnerchrX:112177129..112313322hg18UCSC Ensembl
InnerchrX:112096618..112232811hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg38136195
hg19136194
hg18136194
hg17136194
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv664443, nssv699532, nssv696405, nssv672651, nssv665961, nssv695444, nssv670087, nssv685785, nssv693654, nssv655019
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515695
Frequency
Sample Size2026
Observed Gain10
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer