A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257167



Internal ID21398885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr17:18426930..18557895hg38UCSC Ensembl
chr17:18330244..18461209hg19UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg38130966
hg19130966
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730068
Supporting Variants
SamplesHG00731
Known GenesCCDC144B, FAM106A, KRT16P1, LGALS9C, USP32P2
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257167
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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