A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439864



Internal ID21097417
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:17032718..17033333hg38UCSC Ensembl
chr10:17074717..17075332hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38616
hg19616
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978948
Samples
Known GenesCUBN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439864
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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