A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv930906



Internal ID16224862
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:211312242..211359964hg38UCSC Ensembl
Innerchr2:212176967..212224689hg19UCSC Ensembl
Innerchr2:211885212..211932934hg18UCSC Ensembl
Cytoband2q34
Allele length
AssemblyAllele length
hg3847723
hg1947723
hg1847723
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv584313
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)nssv930906
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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