A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1077770



Internal ID19316675
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:21583132..22699455hg38UCSC Ensembl
chr16:21594453..22710776hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg381116324
hg191116324
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3771023
SamplesKWP1
Known GenesC16orf52, CDR2, EEF2K, IGSF6, LOC653786, METTL9, NPIPB5, OTOA, PDZD9, POLR3E, RRN3P1, RRN3P3, SMG1P1, UQCRC2, VWA3A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nsv1077770
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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