A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6382628



Internal ID21040181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:24839601..24840500hg38UCSC Ensembl
chr5:24839710..24840609hg19UCSC Ensembl
Cytoband5p14.1
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18129139
Samples
Known GenesLOC340107
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6382628
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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