A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1109210



Internal ID19261046
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:52371519..52371584hg38UCSC Ensembl
Outerchr19:52874772..52874837hg19UCSC Ensembl
Cytoband19q13.41
Allele length
AssemblyAllele length
hg3866
hg1966
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3955840
SamplesKWS1
Known GenesZNF880
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1109210
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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