A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125426



Internal ID19264798
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:36642156..36642217hg38UCSC Ensembl
Outerchr7:36681762..36681822hg19UCSC Ensembl
Cytoband7p14.2
Allele length
AssemblyAllele length
hg3862
hg1961
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983598
SamplesKWS2
Known GenesAOAH
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125426
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer