A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv517586



Internal ID15444879
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:128269753..128365512hg38UCSC Ensembl
InnerchrX:127403730..127499490hg19UCSC Ensembl
InnerchrX:127231411..127327171hg18UCSC Ensembl
InnerchrX:127129265..127225025hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg3895760
hg1995761
hg1895761
hg1795761
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv652444, nssv705300, nssv663824, nssv663271
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv517586
Frequency
Sample Size2026
Observed Gain3
Observed Loss1
Observed Complex0
Frequencyn/a


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