A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155199



Internal ID20722239
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:138340517..138346695hg38UCSC Ensembl
chr7:138025262..138031440hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg386179
hg196179
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6415856
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155199
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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