A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258653



Internal ID21400454
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:71546196..71547440hg38UCSC Ensembl
chr12:71939976..71941220hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg381245
hg191245
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730153
Supporting Variants
SamplesNA19239
Known GenesLGR5
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258653
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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