A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011736



Internal ID21921079
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108505316..108505370hg38UCSC Ensembl
chr7:108145760..108145814hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17561742
Samples
Known GenesPNPLA8
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011736
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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