A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18157588



Internal ID20724628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:50782001..50782800hg38UCSC Ensembl
chr7:50849698..50850497hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38800
hg19800
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6619630
Supporting Variants
Samples
Known GenesGRB10
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18157588
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.08348


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