A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11534n54



Internal ID20144958
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:101160859..101238359hg38UCSC Ensembl
chr7:100804140..100881640hg19UCSC Ensembl
chr7:100590860..100668360hg18UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg3877501
hg1977501
hg1877501
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv607976, nsv607977, nsv607975
Samples
Known GenesAP1S1, CLDN15, MOGAT3, NAT16, PLOD3, VGF, ZNHIT1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11534n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer