A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11724n54



Internal ID19003900
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:151054503..151135826hg38UCSC Ensembl
chr7:150751590..150832913hg19UCSC Ensembl
chr7:150382523..150463846hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3881324
hg1981324
hg1881324
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv609014, nsv609012, nsv609013
Samples1780862416_A
Known GenesAGAP3, CDK5, FASTK, SLC4A2, TMUB1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11724n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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