A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6023813



Internal ID21933156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:8656200..8656808hg38UCSC Ensembl
chr12:8808796..8809404hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38609
hg19609
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17617090
Samples
Known GenesMFAP5
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6023813
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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