A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6444297



Internal ID21101850
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13047389..13051810hg38UCSC Ensembl
chr10:13089389..13093810hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg384422
hg194422
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980641
Samples
Known GenesCCDC3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6444297
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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