A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6502213



Internal ID20875456
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82203630..82343926hg38UCSC Ensembl
chr15:82495971..83012565hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38140297
hg19516595
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv18026513
Samples
Known GenesADAMTS7P1, CSPG4P8, EFTUD1, FAM154B, GOLGA6L10, GOLGA6L20, GOLGA6L9, LOC727751, LOC80154, RPS17, RPS17L, UBE2Q2P2, UBE2Q2P3
MethodSequencing
Analysis
Platform
Comments
ReferenceSedlazeck_et_al_2020
Pubmed ID99999999
Accession Number(s)nsv6502213
Frequency
Sample Size19652
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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