A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6142807



Internal ID342008
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:51596000..51604242hg38UCSC Ensembl
chr7:51663696..51671938hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg388243
hg198243
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16995881
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6142807
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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