A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320681



Internal ID20853782
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67695546..67699756hg38UCSC Ensembl
chr1:68161229..68165439hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg384211
hg194211
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062687
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320681
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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