A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606551



Internal ID16393960
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:31550705..31551691hg38UCSC Ensembl
Innerchr7:31590319..31591305hg19UCSC Ensembl
Innerchr7:31556844..31557830hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg38987
hg19987
hg18987
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11264n54
Supporting Variantsnssv1082349
Samples
Known GenesCCDC129
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606551
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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