A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv703256



Internal ID15093222
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
InnerchrX:85851260..85853833hg38UCSC Ensembl
InnerchrX:85106265..85108838hg19UCSC Ensembl
InnerchrX:84992921..84995494hg18UCSC Ensembl
InnerchrX:84912410..84914983hg17UCSC Ensembl
CytobandXq21.2
Allele length
AssemblyAllele length
hg382574
hg192574
hg182574
hg172574
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv519786
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv703256
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