A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11753n54



Internal ID22779648
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:156041367..156071994hg38UCSC Ensembl
chr7:155834061..155864688hg19UCSC Ensembl
chr7:155526822..155557449hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg3830628
hg1930628
hg1830628
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv609165, nsv609166
SamplesNINDS_61
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11753n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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