A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257102



Internal ID21400625
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr12:71546046..71548050hg38UCSC Ensembl
chr12:71939826..71941830hg19UCSC Ensembl
Cytoband12q21.1
Allele length
AssemblyAllele length
hg382005
hg192005
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730153
Supporting Variants
SamplesNA19240
Known GenesLGR5
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257102
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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