A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6517245



Internal ID20890606
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36837922..36949559hg38UCSC Ensembl
chr19:37328824..37440461hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38111638
hg19111638
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046595
Samples
Known GenesZNF345, ZNF568, ZNF790, ZNF829
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6517245
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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