A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18154389



Internal ID20721429
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:136777060..136781075hg38UCSC Ensembl
chr7:136461807..136465822hg19UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg384016
hg194016
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6422875
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18154389
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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