A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6410227



Internal ID21067780
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:162401334..162402055hg38UCSC Ensembl
chr5:161828340..161829061hg19UCSC Ensembl
Cytoband5q34
Allele length
AssemblyAllele length
hg38722
hg19722
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18126702
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6410227
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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