A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256760



Internal ID21400248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195615104..195996875hg38UCSC Ensembl
chr3:195341975..195723746hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38381772
hg19381772
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730152
Supporting Variants
SamplesNA19239
Known GenesMIR570, MIR6829, MUC20, MUC4, SDHAP1, SDHAP2, TNK2
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256760
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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