A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6607938



Internal ID20981009
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:16519118..16536182hg38UCSC Ensembl
chr7:16558743..16575807hg19UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3817065
hg1917065
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236819
Samples
Known GenesLRRC72
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6607938
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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