A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606785



Internal ID16047508
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44227049..44227153hg38UCSC Ensembl
Innerchr7:44266648..44266752hg19UCSC Ensembl
Innerchr7:44233173..44233277hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38105
hg19105
hg18105
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1083445, nssv1083446
Samples
Known GenesCAMK2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606785
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer