A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6412265



Internal ID21069818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:61170158..61178009hg38UCSC Ensembl
chr5:60465985..60473836hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg387852
hg197852
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18133197
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6412265
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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