A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv657663



Internal ID15047629
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:133246963..133297090hg38UCSC Ensembl
Innerchr2:134004535..134054662hg19UCSC Ensembl
Innerchr2:133721005..133771132hg18UCSC Ensembl
Innerchr2:133838267..133888394hg17UCSC Ensembl
Cytoband2q21.2
Allele length
AssemblyAllele length
hg3850128
hg1950128
hg1850128
hg1750128
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516915
Supporting Variants
Samples
Known GenesMIR7853, NCKAP5
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv657663
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