A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17998958



Internal ID20565998
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:30796639..30797335hg38UCSC Ensembl
chr12:30949573..30950269hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38697
hg19697
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6473723
Supporting Variants
Samples
Known GenesLINC00941
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17998958
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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