A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6144770



Internal ID343975
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82340874..82366874hg38UCSC Ensembl
chr15:82633228..83035602hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg3826001
hg19402375
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv175n206
Supporting Variantsnssv17704067
Samples
Known GenesADAMTS7P1, CSPG4P8, GOLGA6L10, GOLGA6L20, GOLGA6L9, LOC727751, LOC80154, RPS17, RPS17L, UBE2Q2P2, UBE2Q2P3
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv6144770
Frequency
Sample Size3202
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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