A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6616656



Internal ID20989727
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108482442..108535056hg38UCSC Ensembl
chr7:108122886..108175500hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3852615
hg1952615
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18147030
Samples
Known GenesPNPLA8
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6616656
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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