A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3764791



Internal ID19312458
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:94767754..94768655hg38UCSC Ensembl
chr2:95433499..95434400hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg38902
hg19902
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1072007
Supporting Variants
SamplesKWP1
Known GenesANKRD20A8P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3764791
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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