A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6003915



Internal ID21913258
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:16136839..16137960hg38UCSC Ensembl
chr8:15994348..15995469hg19UCSC Ensembl
Cytoband8p22
Allele length
AssemblyAllele length
hg381122
hg191122
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563295
Samples
Known GenesMSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6003915
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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