A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6400081



Internal ID21057634
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:120574536..120575131hg38UCSC Ensembl
chr5:119910231..119910826hg19UCSC Ensembl
Cytoband5q23.1
Allele length
AssemblyAllele length
hg38596
hg19596
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124696
Samples
Known GenesPRR16
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6400081
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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