A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1139886



Internal ID19273799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:43968601..43976601hg38UCSC Ensembl
Outerchr7:44008200..44016200hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg388001
hg198001
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978222
SamplesKWS2
Known GenesPOLR2J4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1139886
Frequency
Sample Size2
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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