A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10950



Internal ID15192852
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:21576531..22669350hg38UCSC Ensembl
Outerchr16:21587852..22680671hg19UCSC Ensembl
Outerchr16:21495353..22588172hg18UCSC Ensembl
Outerchr16:21495353..22588172hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381092820
hg191092820
hg181092820
hg171092820
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag1
Merged StatusS
Merged Variantsnsv7280
Supporting Variants
SamplesNA15510
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)nssv10950
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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