A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18158882



Internal ID20725922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:77758454..77764559hg38UCSC Ensembl
chr7:77387771..77393876hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg386106
hg196106
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602930
Supporting Variants
Samples
Known GenesRSBN1L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18158882
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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