A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5847142



Internal ID22622077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64519894..64522627hg38UCSC Ensembl
chr7:63980272..63983005hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg382734
hg192734
Variant TypeOTHER complex
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17508831
Samples
Known GenesZNF680
MethodSequencing
Analysis
Platform
Comments
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nsv5847142
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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