A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615847



Internal ID20988918
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:107555601..107584900hg38UCSC Ensembl
chr7:107196046..107225345hg19UCSC Ensembl
Cytoband7q22.3
Allele length
AssemblyAllele length
hg3829300
hg1929300
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18220362
Samples
Known GenesBCAP29, COG5, DUS4L
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615847
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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