A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327181



Internal ID20860318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:82775535..82780066hg38UCSC Ensembl
chr1:83241218..83245749hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg384532
hg194532
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18064841
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327181
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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