A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1016255



Internal ID19105474
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:56385402..56800076hg38UCSC Ensembl
Innerchr7:56453095..56867769hg19UCSC Ensembl
Innerchr7:56420589..56835263hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38414675
hg19414675
hg18414675
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3661425
Samples
Known GenesDKFZp434L192, LOC100240728, LOC101928401, LOC650226
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1016255
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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