A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017558



Internal ID19106775
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:155264673..155293782hg38UCSC Ensembl
Innerchr7:155056383..155085492hg19UCSC Ensembl
Innerchr7:154687316..154716425hg18UCSC Ensembl
Cytoband7q36.2
Allele length
AssemblyAllele length
hg3829110
hg1929110
hg1829110
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3674695
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)nsv1017558
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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