A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6328549



Internal ID20861697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:67777308..67787211hg38UCSC Ensembl
chr1:68242991..68252894hg19UCSC Ensembl
Cytoband1p31.3
Allele length
AssemblyAllele length
hg389904
hg199904
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18062692
Samples
Known GenesGNG12
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6328549
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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