A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6402981



Internal ID21060534
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:126273387..126281322hg38UCSC Ensembl
chr5:125609080..125617014hg19UCSC Ensembl
Cytoband5q23.2
Allele length
AssemblyAllele length
hg387936
hg197935
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18123719
Samples
Known GenesLOC101927488
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6402981
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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