A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6405165



Internal ID21062718
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:63573698..63580464hg38UCSC Ensembl
chr5:62869525..62876291hg19UCSC Ensembl
Cytoband5q12.1
Allele length
AssemblyAllele length
hg386767
hg196767
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18131382
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6405165
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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