A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765482



Internal ID18968477
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:218865777..218866278hg38UCSC Ensembl
chr2:219730499..219731000hg19UCSC Ensembl
Cytoband2q35
Allele length
AssemblyAllele length
hg38502
hg19502
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072496
Supporting Variants
SamplesKWP1
Known GenesWNT6
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765482
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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