A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6008568



Internal ID21917911
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:98393016..98393178hg38UCSC Ensembl
chr7:98022328..98022490hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg38163
hg19163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17572305
Samples
Known GenesBAIAP2L1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6008568
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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