A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv4003732



Internal ID19188121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:4050080..4050447hg38UCSC Ensembl
Outerchr6:4050314..4050681hg19UCSC Ensembl
Cytoband6p25.2
Allele length
AssemblyAllele length
hg38368
hg19368
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1150431
Supporting Variants
SamplesKWB1
Known GenesPRPF4B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv4003732
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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