A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006065



Internal ID20573105
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97639446..97667640hg38UCSC Ensembl
chr12:98033224..98061418hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3828195
hg1928195
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6463934
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006065
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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