A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16256558



Internal ID21399752
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr2:95761051..96033749hg38UCSC Ensembl
chr2:96426799..96699497hg19UCSC Ensembl
Cytoband2q11.1
Allele length
AssemblyAllele length
hg38272699
hg19272699
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730084
Supporting Variants
SamplesHG00733
Known GenesFAHD2CP, GPAT2, LINC00342
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16256558
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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