A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169552



Internal ID21313785
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:2899285..2964350hg38UCSC Ensembl
Outerchr7:2899170..2965546hg38UCSC Ensembl
Innerchr7:2938919..3003984hg19UCSC Ensembl
Outerchr7:2938804..3005180hg19UCSC Ensembl
Innerchr7:2905445..2970510hg18UCSC Ensembl
Outerchr7:2905330..2971706hg18UCSC Ensembl
Cytoband7p22.2
Allele length
AssemblyAllele length
hg3866377
hg1966377
hg1866377
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245653
SamplesNGO_23
Known GenesCARD11
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169552
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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