A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120142



Internal ID19276552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr4:64853301..64872509hg38UCSC Ensembl
Outerchr4:65719019..65738227hg19UCSC Ensembl
Cytoband4q13.1
Allele length
AssemblyAllele length
hg3819209
hg1919209
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960898
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120142
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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