A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18152790



Internal ID20719830
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112731925..112737158hg38UCSC Ensembl
chr7:112371980..112377213hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg385234
hg195234
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6608042
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18152790
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00018


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