A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv930898



Internal ID15878168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:208156508..208202327hg38UCSC Ensembl
Innerchr2:209021232..209067051hg19UCSC Ensembl
Innerchr2:208729477..208775296hg18UCSC Ensembl
Cytoband2q33.3
Allele length
AssemblyAllele length
hg3845820
hg1945820
hg1845820
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584299
Supporting Variants
Samples
Known GenesC2orf80, CRYGA, LOC100507443
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv930898
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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