A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv692



Internal ID15198623
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:144234571..144274193hg38UCSC Ensembl
Outerchr7:143931664..143971286hg19UCSC Ensembl
Outerchr7:143562597..143602219hg18UCSC Ensembl
Outerchr7:143369312..143408934hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3839623
hg1939623
hg1839623
hg1739623
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv7411
Supporting Variants
SamplesNA19240
Known GenesARHGEF34P, CTAGE4, CTAGE8, OR2A20P, OR2A7, OR2A9P
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)nssv692
Frequency
Sample Size9
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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