A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3566576



Internal ID18864857
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:33009355..33060155hg38UCSC Ensembl
Innerchr19:33500261..33551061hg19UCSC Ensembl
Innerchr19:38192101..38242901hg18UCSC Ensembl
Cytoband19q13.11
Allele length
AssemblyAllele length
hg3850801
hg1950801
hg1850801
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1058846
Supporting Variants
Samples
Known GenesRHPN2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3566576
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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