A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997002



Internal ID20564043
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:112100413..112100870hg38UCSC Ensembl
chr12:112538217..112538674hg19UCSC Ensembl
Cytoband12q24.13
Allele length
AssemblyAllele length
hg38458
hg19458
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6475770
Supporting Variants
Samples
Known GenesNAA25
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997002
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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