A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129322



Internal ID18930827
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:4930499..5027207hg38UCSC Ensembl
Outerchr10:4972691..5069399hg19UCSC Ensembl
Cytoband10p15.1
Allele length
AssemblyAllele length
hg3896709
hg1996709
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv348n106
Supporting Variantsnssv3962755
SamplesKWS1
Known GenesAKR1C1, AKR1C2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129322
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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