A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6615716



Internal ID20988787
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:75738601..75742800hg38UCSC Ensembl
chr7:75367919..75372118hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg384200
hg194200
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6915n223
Supporting Variantsnssv18219026
Samples
Known GenesHIP1
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6615716
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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