A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6447772



Internal ID21105325
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13742054..13742896hg38UCSC Ensembl
chr10:13784054..13784896hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38843
hg19843
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978695
Samples
Known GenesFRMD4A
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6447772
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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