A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110880



Internal ID19248835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:153756744..153756798hg38UCSC Ensembl
Outerchr1:153729220..153729274hg19UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3855
hg1955
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961292
SamplesKWS1
Known GenesINTS3
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110880
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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