A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv4730190



Internal ID21401001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:82337122..82527079hg38UCSC Ensembl
chr15:82629476..83195830hg19UCSC Ensembl
Cytoband15q25.2
Allele length
AssemblyAllele length
hg38189958
hg19566355
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv16258261, nssv16257089, nssv16256212, nssv16258391, nssv16258826, nssv16256019, nssv16256789, nssv16256564
SamplesHG00513, HG00514
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)nsv4730190
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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