A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv18006149



Internal ID20573189
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98624925..98627089hg38UCSC Ensembl
chr12:99018703..99020867hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg382165
hg192165
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6456646
Supporting Variants
Samples
Known GenesIKBIP
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv18006149
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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