A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027872



Internal ID19117090
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:7476493..7561211hg38UCSC Ensembl
Innerchr7:7516124..7600842hg19UCSC Ensembl
Innerchr7:7482649..7567367hg18UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg3884719
hg1984719
hg1884719
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6252n100
Supporting Variantsnssv3655105, nssv3752822, nssv3655104
Samples
Known GenesCOL28A1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027872
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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