A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1120164



Internal ID18913726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:147470236..147470305hg38UCSC Ensembl
Outerchr7:147167328..147167397hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3870
hg1970
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3960924
SamplesKWS1
Known GenesCNTNAP2, MIR548I4
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nsv1120164
Frequency
Sample Size2
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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