A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3997141



Internal ID19186660
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:71193233..71193488hg38UCSC Ensembl
Outerchr3:71242384..71242639hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg38256
hg19256
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1145779
Supporting Variants
SamplesKWB1
Known GenesFOXP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceJohn_et_al_2014
Pubmed ID26484159
Accession Number(s)nssv3997141
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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