A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6316457



Internal ID20849536
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32544002..32549495hg38UCSC Ensembl
chr1:33009603..33015096hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg385494
hg195494
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060468
Samples
Known GenesZBTB8A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6316457
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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