A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6619091



Internal ID20992162
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:87677301..87862700hg38UCSC Ensembl
chr7:87306617..87492015hg19UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38185400
hg19185399
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220767
Samples
Known GenesABCB1, RUNDC3B, SLC25A40
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6619091
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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