A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18236105



Internal ID20803145
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155234743..155283367hg38UCSC Ensembl
chr7:155026453..155075077hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3848625
hg1948625
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6428679
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18236105
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequency0.00013


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