A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18002525



Internal ID20569565
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:70010469..70065964hg38UCSC Ensembl
chr12:70404249..70459744hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg3855496
hg1955496
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6457203
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18002525
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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