A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv6111808



Internal ID22021042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:14927630..18342008hg38UCSC Ensembl
chr16:15021487..18435865hg19UCSC Ensembl
Cytoband16p12.3
Allele length
AssemblyAllele length
hg383414379
hg193414379
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17600713
Samples
Known GenesABCC1, ABCC6, C16orf45, FOPNL, KIAA0430, LOC100288162, MIR3179-1, MIR3179-2, MIR3179-3, MIR3180-1, MIR3180-2, MIR3180-3, MIR3180-4, MIR484, MIR6506, MIR6511A-2, MIR6511B-1, MIR6770-2, MPV17L, MYH11, NDE1, NOMO3, NPIPA1, NPIPA5, NPIPA7, NPIPA8, NTAN1, PDXDC1, PKD1P1, RRN3, XYLT1
MethodSequencing
Analysis
Platform
Comments
ReferenceWu_et_al_2021
Pubmed ID34764282
Accession Number(s)nsv6111808
Frequency
Sample Size405
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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