A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6327693



Internal ID20860834
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:106800561..106836231hg38UCSC Ensembl
chr1:107343183..107378853hg19UCSC Ensembl
Cytoband1p13.3
Allele length
AssemblyAllele length
hg3835671
hg1935671
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18050792
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6327693
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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