A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657677



Internal ID15394329
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:112473564..112477734hg38UCSC Ensembl
InnerchrX:111716792..111720962hg19UCSC Ensembl
InnerchrX:111603448..111607618hg18UCSC Ensembl
InnerchrX:111522937..111527107hg17UCSC Ensembl
CytobandXq23
Allele length
AssemblyAllele length
hg384171
hg194171
hg184171
hg174171
Variant TypeCNV loss
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517690
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657677
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