A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3767603



Internal ID18961022
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr8:67755785..70855717hg38UCSC Ensembl
chr8:68668020..71767952hg19UCSC Ensembl
Cytoband8q13.2
Allele length
AssemblyAllele length
hg383099933
hg193099933
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1068714
Supporting Variants
SamplesKWP1
Known GenesC8orf34, LACTB2, LOC100505718, LOC286189, LOC286190, NCOA2, PRDM14, PREX2, SLCO5A1, SULF1, TRAM1, XKR9
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceThareja_et_al_2015
Pubmed ID25765185
Accession Number(s)nssv3767603
Frequency
Sample Size1
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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