A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv903410



Internal ID16197366
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:6256292..6261988hg38UCSC Ensembl
Innerchr2:6396424..6402120hg19UCSC Ensembl
Innerchr2:6313875..6319571hg18UCSC Ensembl
Cytoband2p25.2
Allele length
AssemblyAllele length
hg385697
hg195697
hg185697
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv580889
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)nssv903410
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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