A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018586



Internal ID19107803
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:109119183..109394088hg38UCSC Ensembl
Innerchr7:108759240..109034145hg19UCSC Ensembl
Innerchr7:108546476..108821381hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38274906
hg19274906
hg18274906
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3656228
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)nsv1018586
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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