A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9526



Internal ID15193102
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:21573703..22671725hg38UCSC Ensembl
Outerchr16:21585024..22683046hg19UCSC Ensembl
Outerchr16:21492525..22590547hg18UCSC Ensembl
Outerchr16:21492525..22590547hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381098023
hg191098023
hg181098023
hg171098023
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7280
Supporting Variants
SamplesNA18507
Known GenesC16orf52, CDR2, EEF2K, IGSF6, LOC100190986, LOC653786, METTL9, NPIPB5, OTOA, PDZD9, POLR3E, RRN3P1, RRN3P3, SMG1P1, UQCRC2, VWA3A
MethodSequencing
AnalysisEnd-sequence pairs were mapped to the human genome assembly (hg17) using a previously described algorithm (Tuzun et al 2005)
PlatformCapillary
Comments
ReferenceKidd_et_al_2008
Pubmed ID18451855
Accession Number(s)nssv9526
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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