A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17998546



Internal ID20565586
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:29028516..29028977hg38UCSC Ensembl
chr12:29181449..29181910hg19UCSC Ensembl
Cytoband12p11.22
Allele length
AssemblyAllele length
hg38462
hg19462
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv6460069
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nssv17998546
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequency0.00078


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