A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18003079



Internal ID20570119
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:7269653..7280809hg38UCSC Ensembl
chr12:7422249..7433405hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg3811157
hg1911157
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6465711
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18003079
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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