A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6333440



Internal ID20866616
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:43247890..43248457hg38UCSC Ensembl
chr1:43713561..43714128hg19UCSC Ensembl
Cytoband1p34.2
Allele length
AssemblyAllele length
hg38568
hg19568
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18060524
Samples
Known GenesWDR65
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6333440
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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