A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6435883



Internal ID21093436
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:96160501..96164800hg38UCSC Ensembl
chr10:97920257..97924556hg19UCSC Ensembl
Cytoband10q24.1
Allele length
AssemblyAllele length
hg384300
hg194300
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985325
Samples
Known GenesZNF518A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6435883
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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