A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6438586



Internal ID21096139
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:128642695..128646500hg38UCSC Ensembl
chr10:130440959..130444764hg19UCSC Ensembl
Cytoband10q26.2
Allele length
AssemblyAllele length
hg383806
hg193806
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17978868
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6438586
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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