A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110879



Internal ID19278369
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:150363045..150388326hg38UCSC Ensembl
Outerchr1:150335521..150360802hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3825282
hg1925282
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961291
SamplesKWS1
Known GenesRPRD2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110879
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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