A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17997777



Internal ID20564817
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:121665262..121677020hg38UCSC Ensembl
chr12:122103168..122114926hg19UCSC Ensembl
Cytoband12q24.31
Allele length
AssemblyAllele length
hg3811759
hg1911759
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6486462
Supporting Variants
Samples
Known GenesMORN3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17997777
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0


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