A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6321079



Internal ID20854181
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33090601..33100000hg38UCSC Ensembl
chr1:33556202..33565601hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg389400
hg199400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060957
Samples
Known GenesADC
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6321079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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