A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6432201



Internal ID21089754
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:139553327..139555295hg38UCSC Ensembl
chr7:139238073..139240041hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381969
hg191969
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18226310
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6432201
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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