A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415017



Internal ID22472887
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40375285..40407109hg38UCSC Ensembl
chr3:40416776..40448600hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3831825
hg1931825
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5906280
Supporting Variants
Samples
Known GenesENTPD3, ENTPD3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415017
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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