A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11572n54



Internal ID22779467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:111203739..111546637hg38UCSC Ensembl
chr7:110843795..111186693hg19UCSC Ensembl
chr7:110631031..110973929hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38342899
hg19342899
hg18342899
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608158, nsv608159, nsv608161
Samples1780854097_A
Known GenesIMMP2L
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11572n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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