A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6395646



Internal ID21053199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:56051010..56051799hg38UCSC Ensembl
chr5:55346837..55347626hg19UCSC Ensembl
Cytoband5q11.2
Allele length
AssemblyAllele length
hg38790
hg19790
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131783
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6395646
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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