A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5856543



Internal ID22631478
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:98878228..98879358hg38UCSC Ensembl
chr12:99272006..99273136hg19UCSC Ensembl
Cytoband12q23.1
Allele length
AssemblyAllele length
hg381131
hg191131
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17467401, nssv17463964
Samples
Known GenesANKS1B
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5856543
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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