A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767966



Internal ID19314415
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:7071568..7078517hg38UCSC Ensembl
chr11:7092799..7099748hg19UCSC Ensembl
Cytoband11p15.4
Allele length
AssemblyAllele length
hg386950
hg196950
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070935
Supporting Variants
SamplesKWP1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767966
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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