A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18147680



Internal ID20714720
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:100095082..100096644hg38UCSC Ensembl
chr7:99692705..99694267hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg381563
hg191563
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6602347
Supporting Variants
Samples
Known GenesMCM7
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18147680
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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