A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18157577



Internal ID20724617
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:50637283..50639527hg38UCSC Ensembl
chr7:50704980..50707224hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg382245
hg192245
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608465
Supporting Variants
Samples
Known GenesGRB10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18157577
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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