A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257819



Internal ID21398337
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:26738682..26763103hg38UCSC Ensembl
chr6:26738777..26763204hg19UCSC Ensembl
Cytoband6p22.2
Allele length
AssemblyAllele length
hg3824422
hg1924428
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730072
Supporting Variants
SamplesHG00513
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257819
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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