A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3765801



Internal ID19310031
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:144497818..144498020hg38UCSC Ensembl
chr2:145255385..145255587hg19UCSC Ensembl
Cytoband2q22.3
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072982
Supporting Variants
SamplesKWP1
Known GenesZEB2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3765801
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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