A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6448603



Internal ID21106156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:114324573..114328548hg38UCSC Ensembl
chr10:116084332..116088307hg19UCSC Ensembl
Cytoband10q25.3
Allele length
AssemblyAllele length
hg383976
hg193976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17977878
Samples
Known GenesAFAP1L2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6448603
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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