A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125323



Internal ID19269370
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:83144053..83171844hg38UCSC Ensembl
Outerchr1:83609736..83637527hg19UCSC Ensembl
Cytoband1p31.1
Allele length
AssemblyAllele length
hg3827792
hg1927792
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962779, nssv3983496
SamplesKWS2, KWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125323
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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