A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18153644



Internal ID20720684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:12022267..12209806hg38UCSC Ensembl
chr7:12061893..12249432hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38187540
hg19187540
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6610233
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18153644
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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