A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17400238



Internal ID22458108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:57133807..57139220hg38UCSC Ensembl
chr19:57645175..57650588hg19UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg385414
hg195414
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5936142
Supporting Variants
Samples
Known GenesZIM3
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17400238
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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