A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6404266



Internal ID21061819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:76722961..76726700hg38UCSC Ensembl
chr5:76018786..76022525hg19UCSC Ensembl
Cytoband5q13.3
Allele length
AssemblyAllele length
hg383740
hg193740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18134493
Samples
Known GenesF2R
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6404266
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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