A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18150941



Internal ID20717981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131865442..131871753hg38UCSC Ensembl
chr7:131550201..131556512hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg386312
hg196312
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6426595
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18150941
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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