A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv683849



Internal ID15420501
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:127016165..127198772hg38UCSC Ensembl
InnerchrX:126150148..126332755hg19UCSC Ensembl
InnerchrX:125977829..126160436hg18UCSC Ensembl
InnerchrX:125875683..126058290hg17UCSC Ensembl
CytobandXq25
Allele length
AssemblyAllele length
hg38182608
hg19182608
hg18182608
hg17182608
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519509
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv683849
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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