A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2995933



Internal ID15582117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr20:16794827..16967672hg38UCSC Ensembl
Innerchr20:16775472..16948317hg19UCSC Ensembl
Cytoband20p12.1
Allele length
AssemblyAllele length
hg38172846
hg19172846
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv483092
Supporting Variants
Samples
Known Genes
MethodBAC aCGH
Analysis
PlatformSpectral Genomics 2600 BAC array
Comments
ReferenceIafrate_et_al_2004
Pubmed ID15286789
Accession Number(s)nssv2995933
Frequency
Sample Size39
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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