A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023682



Internal ID21933025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:95761313..95761370hg38UCSC Ensembl
chr12:96155091..96155148hg19UCSC Ensembl
Cytoband12q22
Allele length
AssemblyAllele length
hg3858
hg1958
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17597975
Samples
Known GenesNTN4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023682
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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