A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17449238



Internal ID22507108
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124336257..124341031hg38UCSC Ensembl
chr7:123976311..123981085hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg384775
hg194775
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979489
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17449238
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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