A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3578983



Internal ID18877264
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:19265603..19324620hg38UCSC Ensembl
Innerchr2:19465364..19524381hg19UCSC Ensembl
Innerchr2:19328845..19387862hg18UCSC Ensembl
Cytoband2p24.1
Allele length
AssemblyAllele length
hg3859018
hg1959018
hg1859018
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1009693
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3578983
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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