A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10949



Internal ID15192851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:21547681..22697177hg38UCSC Ensembl
Outerchr16:21559002..22708498hg19UCSC Ensembl
Outerchr16:21466503..22615999hg18UCSC Ensembl
Outerchr16:21466503..22615999hg17UCSC Ensembl
Cytoband16p12.1
Allele length
AssemblyAllele length
hg381149497
hg191149497
hg181149497
hg171149497
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
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)nssv10949
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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