A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv9532



Internal ID15193096
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:70128805..74391270hg38UCSC Ensembl
Outerchr16:70162708..74425168hg19UCSC Ensembl
Outerchr16:68720209..72982669hg18UCSC Ensembl
Outerchr16:68720209..72982669hg17UCSC Ensembl
Cytoband16q22.1
Allele length
AssemblyAllele length
hg384262466
hg194262461
hg184262461
hg174262461
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7285
Supporting Variants
SamplesNA18507
Known GenesAARS, AP1G1, ATXN1L, C16orf47, CALB2, CHST4, CLEC18C, CMTR2, COG4, DDX19A, DDX19B, DHODH, DHX38, EXOSC6, FUK, HCCAT5, HP, HPR, HYDIN, HYDIN2, IL34, IST1, LOC100132529, LOC100506060, LOC100506083, LOC100506172, LOC101928035, LOC283922, MARVELD3, MTSS1L, PDPR, PHLPP2, PKD1L3, PMFBP1, PSMD7, SF3B3, SNORA70D, SNORD111, SNORD111B, SNORD71, ST3GAL2, TAT, TXNL4B, VAC14, VAC14-AS1, ZFHX3, ZNF19, ZNF23, ZNF821
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)nssv9532
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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