A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv607791



Internal ID16395200
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:90556437..90599724hg38UCSC Ensembl
Innerchr7:90185751..90229038hg19UCSC Ensembl
Innerchr7:90023687..90066974hg18UCSC Ensembl
Cytoband7q21.13
Allele length
AssemblyAllele length
hg3843288
hg1943288
hg1843288
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11499n54
Supporting Variantsnssv1155365
SamplesHGDP00715
Known GenesCDK14
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv607791
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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