A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526696



Internal ID20900057
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:12762469..12777072hg38UCSC Ensembl
chr19:12873283..12887886hg19UCSC Ensembl
Cytoband19p13.2
Allele length
AssemblyAllele length
hg3814604
hg1914604
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18045377
Samples
Known GenesHOOK2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526696
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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