A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11804n54



Internal ID20145228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158818315..159127494hg38UCSC Ensembl
chr7:158611006..158920185hg19UCSC Ensembl
chr7:158303767..158612946hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38309180
hg19309180
hg18309180
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv609422, nsv609420
Samples1780862379_A
Known GenesESYT2, LINC00689, VIPR2, WDR60
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11804n54
Frequency
Sample Size17421
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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