A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008806



Internal ID21918149
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:29629593..29630062hg38UCSC Ensembl
chr10:29918522..29918991hg19UCSC Ensembl
Cytoband10p11.23
Allele length
AssemblyAllele length
hg38470
hg19470
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17586524
Samples
Known GenesSVIL
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008806
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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