A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18158892



Internal ID20725932
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:78046929..78052191hg38UCSC Ensembl
chr7:77676246..77681508hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg385263
hg195263
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6600130
Supporting Variants
Samples
Known GenesMAGI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18158892
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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