A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1028902



Internal ID19118121
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:137042389..137174057hg38UCSC Ensembl
Innerchr7:136727136..136858804hg19UCSC Ensembl
Innerchr7:136377676..136509344hg18UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg38131669
hg19131669
hg18131669
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3664239
Samples
Known GenesLOC349160
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1028902
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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