A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11265n54



Internal ID22779160
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:31550705..31552257hg38UCSC Ensembl
chr7:31590319..31591871hg19UCSC Ensembl
chr7:31556844..31558396hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381553
hg191553
hg181553
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv606557, nsv606569, nsv606556, nsv606558, nsv606561, nsv606562, nsv606568, nsv606570, nsv606564
Samples
Known GenesCCDC129
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11265n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss189
Observed Complex0
Frequencyn/a


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