A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169959



Internal ID21314020
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44746590..44811408hg38UCSC Ensembl
Outerchr7:44738204..44814903hg38UCSC Ensembl
Innerchr7:44786189..44851007hg19UCSC Ensembl
Outerchr7:44777803..44854502hg19UCSC Ensembl
Innerchr7:44752714..44817532hg18UCSC Ensembl
Outerchr7:44744328..44821027hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3876700
hg1976700
hg1876700
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14245072
SamplesPML_1
Known GenesPPIA, ZMIZ2
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169959
Frequency
Sample Size93
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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