A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6329950



Internal ID20863104
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:221393090..221399502hg38UCSC Ensembl
chr1:221566432..221572844hg19UCSC Ensembl
Cytoband1q41
Allele length
AssemblyAllele length
hg386413
hg196413
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18058020
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6329950
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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