A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6359595



Internal ID21017148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:40375285..40407114hg38UCSC Ensembl
chr3:40416776..40448605hg19UCSC Ensembl
Cytoband3p22.1
Allele length
AssemblyAllele length
hg3831830
hg1931830
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18099138
Samples
Known GenesENTPD3, ENTPD3-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6359595
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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