A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6440009



Internal ID21097562
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:129782637..129783648hg38UCSC Ensembl
chr10:131580901..131581912hg19UCSC Ensembl
Cytoband10q26.3
Allele length
AssemblyAllele length
hg381012
hg191012
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980584
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6440009
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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