A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1110976



Internal ID18903885
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:139357931..139357990hg38UCSC Ensembl
Outerchr7:139042677..139042736hg19UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3961404
SamplesKWS1
Known GenesC7orf55-LUC7L2, LUC7L2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1110976
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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