A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6604513



Internal ID20977584
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87601503..87611633hg38UCSC Ensembl
chr7:87230819..87240949hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg3810131
hg1910131
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18229525
Samples
Known GenesABCB1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6604513
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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