A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257887



Internal ID21400242
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:195652372..195996876hg38UCSC Ensembl
chr3:195379243..195723747hg19UCSC Ensembl
Cytoband3q29
Allele length
AssemblyAllele length
hg38344505
hg19344505
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)nssv16257887
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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