A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6323986



Internal ID20857109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:38957699..38966883hg38UCSC Ensembl
chr1:39423371..39432555hg19UCSC Ensembl
Cytoband1p34.3
Allele length
AssemblyAllele length
hg389185
hg199185
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060075
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6323986
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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