A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6009266



Internal ID21918609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7302866..7302994hg38UCSC Ensembl
chr6:7303099..7303227hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg38129
hg19129
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17569093
Samples
Known GenesSSR1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6009266
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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