A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6442141



Internal ID21099694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:34038034..34047009hg38UCSC Ensembl
chr10:34326962..34335937hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg388976
hg198976
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17979808
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6442141
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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