A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6361156



Internal ID21018709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:8680320..8728511hg38UCSC Ensembl
chr3:8722006..8770197hg19UCSC Ensembl
Cytoband3p25.3
Allele length
AssemblyAllele length
hg3848192
hg1948192
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18104023
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6361156
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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