A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129419



Internal ID19280790
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:104675977..104702672hg38UCSC Ensembl
Outerchr4:105597134..105623829hg19UCSC Ensembl
Cytoband4q24
Allele length
AssemblyAllele length
hg3826696
hg1926696
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962861
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129419
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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