A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17393610



Internal ID22451480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr19:40195435..40195511hg38UCSC Ensembl
chr19:40701342..40701418hg19UCSC Ensembl
Cytoband19q13.2
Allele length
AssemblyAllele length
hg3877
hg1977
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5947050
Supporting Variants
Samples
Known GenesMAP3K10
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17393610
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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