A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027409



Internal ID19116628
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:54118232..54129851hg38UCSC Ensembl
Innerchr7:54185925..54197544hg19UCSC Ensembl
Innerchr7:54153419..54165038hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg3811620
hg1911620
hg1811620
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6354n100
Supporting Variantsnssv3661313, nssv3661314, nssv3661315
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)nsv1027409
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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