A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17350347



Internal ID22576016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:82249850..82337035hg38UCSC Ensembl
chr12:82643629..82730814hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg3887186
hg1987186
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5944740
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17350347
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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