A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116472



Internal ID19263878
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr3:22709960..22741078hg38UCSC Ensembl
Outerchr3:22751451..22782569hg19UCSC Ensembl
Cytoband3p24.3
Allele length
AssemblyAllele length
hg3831119
hg1931119
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv2497n106
Supporting Variantsnssv3978653
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116472
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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