A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17442963



Internal ID22500833
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:8735527..9440147hg38UCSC Ensembl
chr7:8775157..9479777hg19UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38704621
hg19704621
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5973436
Supporting Variants
Samples
Known GenesNXPH1
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17442963
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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