A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6525558



Internal ID20898919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:37698729..37699365hg38UCSC Ensembl
chr19:38189630..38190266hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38637
hg19637
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18046670
Samples
Known GenesZNF607
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6525558
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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