A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17463681



Internal ID22521567
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:81792444..81802153hg38UCSC Ensembl
chr12:82186223..82195932hg19UCSC Ensembl
Cytoband12q21.31
Allele length
AssemblyAllele length
hg389710
hg199710
Variant TypeOTHER copy number variation
Copy Number2
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5866444
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17463681
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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