A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv14245194



Internal ID21306470
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76680351..76696439hg38UCSC Ensembl
Outerchr7:76678906..76696440hg38UCSC Ensembl
Innerchr7:76309668..76325756hg19UCSC Ensembl
Outerchr7:76308223..76325757hg19UCSC Ensembl
Innerchr7:76147604..76163692hg18UCSC Ensembl
Outerchr7:76146159..76163693hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3817535
hg1917535
hg1817535
Variant TypeCNV duplication
Copy Number3
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv3170160
Supporting Variants
SamplesNGO_28
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nssv14245194
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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