A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5944761



Internal ID22720230
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:97431258..97441997hg38UCSC Ensembl
chr12:97825036..97835775hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg3810740
hg1910740
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17350693
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5944761
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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