A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18229339



Internal ID20796379
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:36362101..36401500hg38UCSC Ensembl
chr7:36401710..36441109hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3839400
hg1939400
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608921
Supporting Variants
Samples
Known GenesANLN, KIAA0895
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18229339
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00081


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