A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv916442



Internal ID16210398
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:120429487..120445935hg38UCSC Ensembl
Innerchr2:121187063..121203511hg19UCSC Ensembl
Innerchr2:120903533..120919981hg18UCSC Ensembl
Cytoband2q14.2
Allele length
AssemblyAllele length
hg3816449
hg1916449
hg1816449
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv582795
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv916442
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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