A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1055695



Internal ID19144914
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:29333400..29368257hg38UCSC Ensembl
Innerchr19:29824307..29859164hg19UCSC Ensembl
Innerchr19:34516147..34551004hg18UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg3834858
hg1934858
hg1834858
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3566528
Samples
Known GenesLOC284395
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1055695
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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