A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17354702



Internal ID22580371
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:12704264..12704447hg38UCSC Ensembl
chr12:12857198..12857381hg19UCSC Ensembl
Cytoband12p13.1
Allele length
AssemblyAllele length
hg38184
hg19184
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5919691
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17354702
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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