A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3739642



Internal ID19037923
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:21188166..21293216hg38UCSC Ensembl
Innerchr3:21229658..21334708hg19UCSC Ensembl
Innerchr3:21204662..21309712hg18UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg38105051
hg19105051
hg18105051
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1013006
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)nssv3739642
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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