A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3960827



Internal ID18859178
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:49070262..49102160hg38UCSC Ensembl
Outerchr10:50278307..50310205hg19UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg3831899
hg1931899
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1120083
Supporting Variants
SamplesKWS1
Known GenesVSTM4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3960827
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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