A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671840



Internal ID15061806
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:85666713..85907957hg38UCSC Ensembl
InnerchrX:84921718..85162962hg19UCSC Ensembl
InnerchrX:84808374..85049618hg18UCSC Ensembl
InnerchrX:84727863..84969107hg17UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg38241245
hg19241245
hg18241245
hg17241245
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519786
Supporting Variants
Samples
Known GenesCHM
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671840
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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