A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6344027



Internal ID21001580
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:36066364..36108773hg38UCSC Ensembl
chr2:36293507..36335916hg19UCSC Ensembl
Cytoband2p22.3
Allele length
AssemblyAllele length
hg3842410
hg1942410
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18089016
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6344027
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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