A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256019



Internal ID21398505
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82339922..82477207hg38UCSC Ensembl
chr15:82632276..83145932hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38137286
hg19513657
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730190
Supporting Variants
SamplesHG00514
Known GenesADAMTS7P1, CSPG4P8, GOLGA6L10, GOLGA6L20, GOLGA6L9, LOC727751, LOC80154, RPS17, RPS17L, UBE2Q2P2, UBE2Q2P3
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256019
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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