A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1024141



Internal ID19113358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:53193651..53505442hg38UCSC Ensembl
Innerchr7:53261344..53573135hg19UCSC Ensembl
Innerchr7:53228838..53540629hg18UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg38311792
hg19311792
hg18311792
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661287, nssv3661288
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)nsv1024141
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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