A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767935



Internal ID18964437
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:237691756..237692457hg38UCSC Ensembl
chr2:238600399..238601100hg19UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg38702
hg19702
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1073026
Supporting Variants
SamplesKWP1
Known GenesLRRFIP1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767935
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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