A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606766



Internal ID16394175
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:44226790..44227322hg38UCSC Ensembl
Innerchr7:44266389..44266921hg19UCSC Ensembl
Innerchr7:44232914..44233446hg18UCSC Ensembl
Cytoband7p13
Allele length
AssemblyAllele length
hg38533
hg19533
hg18533
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11303n54
Supporting Variantsnssv1083269, nssv1083270
Samples
Known GenesCAMK2B
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606766
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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