A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6453242



Internal ID21110795
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:7922714..7923300hg38UCSC Ensembl
chr10:7964677..7965263hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg38587
hg19587
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17983588
Samples
Known GenesTAF3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6453242
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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