A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327599



Internal ID20860739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:73442660..73467891hg38UCSC Ensembl
chr1:73908343..73933574hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3825232
hg1925232
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18063719
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327599
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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