A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3955097



Internal ID21375166
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36505307..36505561hg38UCSC Ensembl
chr2:36732450..36732704hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg38255
hg19255
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv15177028
SamplesHG002
Known GenesCRIM1
MethodSequencing
Analysis
Platform
Comments
ReferenceWenger_et_al_2019
Pubmed ID31406327
Accession Number(s)nsv3955097
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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