A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1083444



Internal ID15589944
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44226995..44238106hg38UCSC Ensembl
Innerchr7:44266594..44277705hg19UCSC Ensembl
Innerchr7:44233119..44244230hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg3811112
hg1911112
hg1811112
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv606784
Supporting Variants
Samples
Known GenesCAMK2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1083444
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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