A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3978748



Internal ID19237698
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 StatusS
Merged Variantsnsv1116568
Supporting Variants
SamplesKWS2
Known Genes
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3978748
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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