A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv999025



Internal ID19158561
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:20696752..21000757hg38UCSC Ensembl
Innerchr3:20738244..21042249hg19UCSC Ensembl
Innerchr3:20713248..21017253hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38304006
hg19304006
hg18304006
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3739640
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)nsv999025
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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