A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17360561



Internal ID22586230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:31366878..31367486hg38UCSC Ensembl
chr12:31519812..31520420hg19UCSC Ensembl
Cytoband12p11.21
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5925517
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17360561
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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