A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6617910



Internal ID20990981
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:64593536..64719409hg38UCSC Ensembl
chr7:64053914..64179787hg19UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38125874
hg19125874
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18219716
Samples
Known GenesLOC100128885, MIR6839, ZNF107
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6617910
Frequency
Sample Size19652
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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