A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1125427



Internal ID19255876
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:44785700..44785755hg38UCSC Ensembl
Outerchr7:44825299..44825354hg19UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3856
hg1956
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3983599
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1125427
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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