A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18046156



Internal ID20613196
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36416491..37213522hg38UCSC Ensembl
chr19:36907393..37704424hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38797032
hg19797032
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6535180
Supporting Variants
Samples
Known GenesLOC644189, LOC728752, ZFP82, ZNF260, ZNF345, ZNF382, ZNF420, ZNF461, ZNF529, ZNF566, ZNF567, ZNF568, ZNF585A, ZNF585B, ZNF790, ZNF790-AS1, ZNF829, ZNF850
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18046156
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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