A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6067304



Internal ID21976537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:50725795..50725795hg38UCSC Ensembl
chr6:50693508..50693508hg19UCSC Ensembl
Cytoband6p12.3
Allele length
AssemblyAllele length
hg38313
hg19313
Variant TypeCNV insertion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17559255
Samples
Known GenesTFAP2D
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6067304
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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