A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120069



Internal ID18914639
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr1:10978049..10978251hg38UCSC Ensembl
Outerchr1:11038106..11038308hg19UCSC Ensembl
Cytoband1p36.22
Allele length
AssemblyAllele length
hg38203
hg19203
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960811
SamplesKWS1
Known GenesC1orf127
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120069
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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