A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6449144



Internal ID21106697
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:116351548..116352280hg38UCSC Ensembl
chr10:118111060..118111792hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg38733
hg19733
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978250
Samples
Known GenesCCDC172
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6449144
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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