A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025387



Internal ID19114605
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:92851095..92874710hg38UCSC Ensembl
Innerchr7:92480409..92504024hg19UCSC Ensembl
Innerchr7:92318345..92341960hg18UCSC Ensembl
Cytoband7q21.2
Allele length
AssemblyAllele length
hg3823616
hg1923616
hg1823616
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655249, nssv3655248
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)nsv1025387
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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