A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6004812



Internal ID21914155
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:112124186..112132811hg38UCSC Ensembl
chr7:111764241..111772866hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg388626
hg198626
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17563279
Samples
Known GenesDOCK4
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6004812
Frequency
Sample Size405
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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