A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024509



Internal ID19113726
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:89920171..90082508hg38UCSC Ensembl
Innerchr7:89549485..89711822hg19UCSC Ensembl
Innerchr7:89387421..89549758hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg38162338
hg19162338
hg18162338
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3655222
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)nsv1024509
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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