A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6141707



Internal ID340904
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:102328779..102382779hg38UCSC Ensembl
chr7:101969196..102023226hg19UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3854001
hg1954031
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17000198
Samples
Known GenesLOC100289561, LOC100630923, SPDYE6
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6141707
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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