A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6608938



Internal ID20982009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:104816020..104829118hg38UCSC Ensembl
chr7:104456467..104469565hg19UCSC Ensembl
Cytoband7q22.2
Allele length
AssemblyAllele length
hg3813099
hg1913099
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18152016
Samples
Known GenesLHFPL3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6608938
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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