A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3772275



Internal ID18966453
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:61276227..61277328hg38UCSC Ensembl
chr11:61043699..61044800hg19UCSC Ensembl
Cytoband11q12.2
Allele length
AssemblyAllele length
hg381102
hg191102
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1070460
Supporting Variants
SamplesKWP1
Known GenesVWCE
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3772275
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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