A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6335098



Internal ID20868289
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32467101..32468000hg38UCSC Ensembl
chr1:32932702..32933601hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg38900
hg19900
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060460
Samples
Known GenesZBTB8B
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6335098
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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