A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18218128



Internal ID20785168
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:121271285..121298314hg38UCSC Ensembl
chr7:120911339..120938368hg19UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3827030
hg1927030
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610345
Supporting Variants
Samples
Known GenesCPED1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18218128
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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