A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452283



Internal ID21109836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:12095578..12121488hg38UCSC Ensembl
chr10:12137577..12163487hg19UCSC Ensembl
Cytoband10p14
Allele length
AssemblyAllele length
hg3825911
hg1925911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980515
Samples
Known GenesDHTKD1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452283
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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