A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv16257574



Internal ID21399624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:54232567..54321398hg38UCSC Ensembl
chr7:54300260..54389091hg19UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3888832
hg1988832
Variant TypeOTHER inversion
Copy Number
Allele StateHomozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv4730048
Supporting Variants
SamplesHG00733
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceHanlon_et_al_2021
Pubmed ID34332539
Accession Number(s)nssv16257574
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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