A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3998240



Internal ID18840839
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:30526444..30526745hg38UCSC Ensembl
Outerchr19:31017351..31017652hg19UCSC Ensembl
Cytoband19q12
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1146881
Supporting Variants
SamplesKWB1
Known GenesZNF536
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3998240
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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