A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6597372



Internal ID20970443
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:36322830..37322723hg38UCSC Ensembl
chr19:36813732..37813625hg19UCSC Ensembl
Cytoband19q13.12
Allele length
AssemblyAllele length
hg38999894
hg19999894
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18247680
Samples
Known GenesLINC00665, LOC284412, LOC644189, LOC728752, ZFP14, ZFP82, ZNF260, ZNF345, ZNF382, ZNF383, 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)nsv6597372
Frequency
Sample Size19652
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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