A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18004262



Internal ID20571302
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:85245901..85249400hg38UCSC Ensembl
chr12:85639679..85643178hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg383500
hg193500
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6464675
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18004262
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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