A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6439961



Internal ID21097514
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:69471033..69478254hg38UCSC Ensembl
chr10:71230789..71238010hg19UCSC Ensembl
Cytoband10q22.1
Allele length
AssemblyAllele length
hg387222
hg197222
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv800n223
Supporting Variantsnssv17983070
Samples
Known GenesTSPAN15
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6439961
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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