A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1143906



Internal ID18910083
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr19:4968989..4969689hg38UCSC Ensembl
Outerchr19:4969000..4969700hg19UCSC Ensembl
Cytoband19p13.3
Allele length
AssemblyAllele length
hg38701
hg19701
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3994610
SamplesKWS1
Known GenesKDM4B
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1143906
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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