A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16258019



Internal ID21399051
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:97436188..97461596hg38UCSC Ensembl
chr7:97065500..97090908hg19UCSC Ensembl
Cytoband7q21.3
Allele length
AssemblyAllele length
hg3825409
hg1925409
Variant TypeOTHER inversion
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730264
Supporting Variants
SamplesHG00731
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16258019
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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