A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617487



Internal ID20990558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:103857167..103875790hg38UCSC Ensembl
chr7:103497614..103516237hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3818624
hg1918624
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18222428
Samples
Known GenesRELN
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617487
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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