A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6535180



Internal ID20908541
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 StatusM
Merged Variants
Supporting Variantsnssv18046156
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)nsv6535180
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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