A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1129435



Internal ID19254877
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:23776047..23798544hg38UCSC Ensembl
Outerchr7:23815666..23838163hg19UCSC Ensembl
Cytoband7p15.3
Allele length
AssemblyAllele length
hg3822498
hg1922498
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3962881
SamplesKWS1
Known GenesSTK31
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1129435
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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