A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1009693



Internal ID19098911
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 StatusM
Merged Variants
Supporting Variantsnssv3578983
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)nsv1009693
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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