A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6341083



Internal ID20998636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:66116613..66138958hg38UCSC Ensembl
chr2:66343746..66366090hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3822346
hg1922345
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18090035
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6341083
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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