A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606756



Internal ID16047479
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44226585..44227212hg38UCSC Ensembl
Innerchr7:44266184..44266811hg19UCSC Ensembl
Innerchr7:44232709..44233336hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38628
hg19628
hg18628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1083236
Samples
Known GenesCAMK2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606756
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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