A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10085



Internal ID15196026
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:21553002..22691636hg38UCSC Ensembl
Outerchr16:21564323..22702957hg19UCSC Ensembl
Outerchr16:21471824..22610458hg18UCSC Ensembl
Outerchr16:21471824..22610458hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381138635
hg191138635
hg181138635
hg171138635
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7280
Supporting Variants
SamplesNA18956
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)nssv10085
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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