A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17419488



Internal ID22477358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr5:88697955..88701084hg38UCSC Ensembl
chr5:87993772..87996901hg19UCSC Ensembl
Cytoband5q14.3
Allele length
AssemblyAllele length
hg383130
hg193130
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5979157
Supporting Variants
Samples
Known Genes
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17419488
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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