A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1023789



Internal ID19113006
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:119163405..119214525hg38UCSC Ensembl
Innerchr7:118803459..118854579hg19UCSC Ensembl
Innerchr7:118590695..118641815hg18UCSC Ensembl
Cytoband7q31.31
Allele length
AssemblyAllele length
hg3851121
hg1951121
hg1851121
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3662069
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1023789
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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