A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335799



Internal ID20993352
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:37236109..37237598hg38UCSC Ensembl
chr2:37463252..37464741hg19UCSC Ensembl
Cytoband2p22.2
Allele length
AssemblyAllele length
hg381490
hg191490
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089092
Samples
Known GenesNDUFAF7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335799
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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