A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17430948



Internal ID22488818
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:155157535..155170902hg38UCSC Ensembl
chr7:154949245..154962612hg19UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3813368
hg1913368
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5975912
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17430948
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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