A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5946064



Internal ID22721548
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95344338..95344634hg38UCSC Ensembl
chr12:95738114..95738410hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg38297
hg19297
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350302
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5946064
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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