A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978979



Internal ID19240334
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:175231433..175232798hg38UCSC Ensembl
Outerchr1:175200569..175201934hg19UCSC Ensembl
Cytoband1q25.1
Allele length
AssemblyAllele length
hg381366
hg191366
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1140267
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978979
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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