A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3570679



Internal ID18868960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:24196288..24320971hg38UCSC Ensembl
Innerchr19:24379090..24503773hg19UCSC Ensembl
Innerchr19:24170930..24295613hg18UCSC Ensembl
Cytoband19p11
Allele length
AssemblyAllele length
hg38124684
hg19124684
hg18124684
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1064250
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)nssv3570679
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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