A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6618046



Internal ID20991117
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64520099..64701532hg38UCSC Ensembl
chr7:63980477..64161910hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38181434
hg19181434
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18232168
Samples
Known GenesLOC100128885, LOC641746, MIR6839, ZNF107, ZNF680
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6618046
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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