A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18220937



Internal ID20787977
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:55317654..55578429hg38UCSC Ensembl
chr7:55385347..55646122hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38260776
hg19260776
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6604878
Supporting Variants
Samples
Known GenesLANCL2, VOPP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18220937
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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