A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17415206



Internal ID22473076
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:14742874..15551121hg38UCSC Ensembl
chr3:14784381..15592628hg19UCSC Ensembl
Cytoband3p25.1
Allele length
AssemblyAllele length
hg38808248
hg19808248
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5968065
Supporting Variants
Samples
Known GenesC3orf20, CAPN7, COL6A4P1, COLQ, EAF1, FGD5, FGD5-AS1, METTL6, MIR4270, MRPS25, NR2C2, SH3BP5, SH3BP5-AS1, ZFYVE20
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17415206
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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