A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17424806



Internal ID22482676
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:15499354..15500007hg38UCSC Ensembl
chr3:15540861..15541514hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38654
hg19654
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5976829
Supporting Variants
Samples
Known GenesCOLQ
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17424806
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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