A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6352684



Internal ID21010237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:57912316..57913128hg38UCSC Ensembl
chr2:58139451..58140263hg19UCSC Ensembl
Cytoband2p16.1
Allele length
AssemblyAllele length
hg38813
hg19813
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18088493
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6352684
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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