A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6610247



Internal ID20983318
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:79156108..79181291hg38UCSC Ensembl
chr7:78785424..78810607hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3825184
hg1925184
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18236357
Samples
Known GenesMAGI2
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6610247
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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