A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6011872



Internal ID21921215
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149556132..149597424hg38UCSC Ensembl
chr7:149253223..149294515hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3841293
hg1941293
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17576014
Samples
Known GenesZNF767
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6011872
Frequency
Sample Size405
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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