A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3981119



Internal ID18878670
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:3478602..3480502hg38UCSC Ensembl
Outerchr19:3478600..3480500hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg381901
hg191901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118805
Supporting Variants
SamplesKWS1
Known GenesC19orf77
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3981119
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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