A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6396267



Internal ID21053820
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:77679709..77682685hg38UCSC Ensembl
chr5:76975534..76978510hg19UCSC Ensembl
Cytoband5q14.1
Allele length
AssemblyAllele length
hg382977
hg192977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18135135
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6396267
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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