A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767938



Internal ID18964602
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:46699160..46699461hg38UCSC Ensembl
chr2:46926299..46926600hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38302
hg19302
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072938
Supporting Variants
SamplesKWP1
Known GenesSOCS5
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767938
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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