A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6320344



Internal ID20853442
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:32568554..32573126hg38UCSC Ensembl
chr1:33034155..33038727hg19UCSC Ensembl
Cytoband1p35.1
Allele length
AssemblyAllele length
hg384573
hg194573
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060473
Samples
Known GenesZBTB8A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6320344
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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