A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1027807



Internal ID19117025
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:33091063..33150979hg38UCSC Ensembl
Innerchr7:33130675..33190591hg19UCSC Ensembl
Innerchr7:33097200..33157116hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3859917
hg1959917
hg1859917
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6319n100
Supporting Variantsnssv3752947
Samples
Known GenesBBS9, RP9
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1027807
Frequency
Sample Size11257
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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