A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6452187



Internal ID21109740
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:4387907..4454196hg38UCSC Ensembl
chr10:4430099..4496388hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3866290
hg1966290
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17980304
Samples
Known GenesLINC00703
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6452187
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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