A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1021471



Internal ID19110689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:15708058..15726859hg38UCSC Ensembl
Innerchr7:15747683..15766484hg19UCSC Ensembl
Innerchr7:15714208..15733009hg18UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3818802
hg1918802
hg1818802
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643186, nssv3643185
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)nsv1021471
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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