A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1116568



Internal ID19264048
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:85255639..85272407hg38UCSC Ensembl
Outerchr7:84884955..84901723hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3816769
hg1916769
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3978748
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1116568
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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