A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987824



Internal ID19217153
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:91040251..91040331hg38UCSC Ensembl
Outerchr1:91505808..91505888hg19UCSC Ensembl
Cytoband1p22.2
Allele length
AssemblyAllele length
hg3881
hg1981
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133027
Supporting Variants
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987824
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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