A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6441835



Internal ID21099388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:91798201..91799000hg38UCSC Ensembl
chr10:93557958..93558757hg19UCSC Ensembl
Cytoband10q23.32
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17985371
Samples
Known GenesTNKS2, TNKS2-AS1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6441835
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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