A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6339055



Internal ID20996608
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:65958401..65968800hg38UCSC Ensembl
chr2:66185535..66195934hg19UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3810400
hg1910400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3910n223
Supporting Variantsnssv18090013
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6339055
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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