A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18155511



Internal ID20722551
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:48675712..48689954hg38UCSC Ensembl
chr7:48715308..48729550hg19UCSC Ensembl
Cytoband7p12.3
Allele length
AssemblyAllele length
hg3814243
hg1914243
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6618846
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18155511
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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