A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6325359



Internal ID20858490
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:33641664..33641979hg38UCSC Ensembl
chr1:34107264..34107579hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38316
hg19316
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060979
Samples
Known GenesCSMD2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6325359
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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