A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18231916



Internal ID20798956
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:39701308..39934989hg38UCSC Ensembl
chr7:39740907..39974588hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38233682
hg19233682
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6611127
Supporting Variants
Samples
Known GenesLINC00265, RALA
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18231916
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0


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