A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025620



Internal ID19114838
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90475310..90538525hg38UCSC Ensembl
Innerchr7:90104624..90167839hg19UCSC Ensembl
Innerchr7:89942560..90005775hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3863216
hg1963216
hg1863216
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6532n100
Supporting Variantsnssv3655229
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)nsv1025620
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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