A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110971



Internal ID19278432
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr6:125772722..125772863hg38UCSC Ensembl
Outerchr6:126093868..126094009hg19UCSC Ensembl
Cytoband6q22.31
Allele length
AssemblyAllele length
hg38142
hg19142
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961398
SamplesKWS1
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110971
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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