A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125320



Internal ID19270574
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:21013565..21013655hg38UCSC Ensembl
Outerchr1:21340058..21340148hg19UCSC Ensembl
Cytoband1p36.12
Allele length
AssemblyAllele length
hg3891
hg1991
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983492
SamplesKWS2
Known GenesEIF4G3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125320
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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