A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv10533



Internal ID15195579
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:6006077..6756301hg38UCSC Ensembl
Outerchr7:6045708..6795932hg19UCSC Ensembl
Outerchr7:6012234..6762457hg18UCSC Ensembl
Outerchr7:5818949..6569172hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38750225
hg19750225
hg18750224
hg17750224
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7392
Supporting Variants
SamplesNA18956
Known GenesAIMP2, ANKRD61, C7orf26, CYTH3, DAGLB, EIF2AK1, FAM220A, GRID2IP, KDELR2, PMS2, PMS2CL, RAC1, RSPH10B, RSPH10B2, USP42, ZDHHC4, ZNF12, ZNF316, ZNF853
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)nssv10533
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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