A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6360377



Internal ID21017930
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:131003318..131003802hg38UCSC Ensembl
chr3:130722162..130722646hg19UCSC Ensembl
Cytoband3q22.1
Allele length
AssemblyAllele length
hg38485
hg19485
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18094244
Samples
Known GenesATP2C1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6360377
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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