A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3987818



Internal ID18870581
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:23873238..23876852hg38UCSC Ensembl
Outerchr1:24199728..24203342hg19UCSC Ensembl
Cytoband1p36.11
Allele length
AssemblyAllele length
hg383615
hg193615
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133021
Supporting Variants
SamplesKWS1
Known GenesCNR2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3987818
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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