A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6355089



Internal ID21012642
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:78139580..78376257hg38UCSC Ensembl
chr2:78366706..78603383hg19UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg38236678
hg19236678
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090725
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6355089
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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