A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5923557



Internal ID22698784
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:17436309..17448426hg38UCSC Ensembl
chr12:17589243..17601360hg19UCSC Ensembl
Cytoband12p12.3
Allele length
AssemblyAllele length
hg3812118
hg1912118
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17358712
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5923557
Frequency
Sample Size914
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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