A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6526997



Internal ID20900358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:44079537..44079758hg38UCSC Ensembl
chr19:44583690..44583911hg19UCSC Ensembl
Cytoband19q13.31
Allele length
AssemblyAllele length
hg38222
hg19222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18048142
Samples
Known GenesZNF284
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6526997
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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