A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv606556



Internal ID16393965
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:31550705..31552108hg38UCSC Ensembl
Innerchr7:31590319..31591722hg19UCSC Ensembl
Innerchr7:31556844..31558247hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381404
hg191404
hg181404
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv11265n54
Supporting Variantsnssv1082356
Samples
Known GenesCCDC129
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv606556
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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