A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5860961



Internal ID22635896
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:70396892..70398891hg38UCSC Ensembl
chr12:70790672..70792671hg19UCSC Ensembl
Cytoband12q15
Allele length
AssemblyAllele length
hg382000
hg192000
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17465436
Samples
Known GenesKCNMB4
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5860961
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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