A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382525



Internal ID21040078
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:10714739..10719747hg38UCSC Ensembl
chr5:10714851..10719859hg19UCSC Ensembl
Cytoband5p15.2
Allele length
AssemblyAllele length
hg385009
hg195009
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18124198
Samples
Known GenesDAP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382525
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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