A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355395



Internal ID21012948
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:41934279..41939769hg38UCSC Ensembl
chr2:42161419..42166909hg19UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg385491
hg195491
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18087859
Samples
Known GenesC2orf91
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355395
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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