A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5925391



Internal ID22700618
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:6568662..6568954hg38UCSC Ensembl
chr12:6677828..6678120hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38293
hg19293
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17357460
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5925391
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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