A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120063



Internal ID18932156
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:4983284..5803122hg38UCSC Ensembl
Outerchr7:5022915..5842753hg19UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38819839
hg19819839
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3482n106
Supporting Variantsnssv3960805
SamplesKWS1
Known GenesACTB, FBXL18, FSCN1, MIR589, MIR6874, RBAK, RBAKDN, RBAK-RBAKDN, RNF216, RNF216-IT1, RNF216P1, SLC29A4, TNRC18, WIPI2, ZNF890P
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120063
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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