A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17998759



Internal ID20565799
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:122954648..122970439hg38UCSC Ensembl
chr12:123439195..123454986hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3815792
hg1915792
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6476153
Supporting Variants
Samples
Known GenesABCB9
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17998759
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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