A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv726n54



Internal ID22768621
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:194802203..194880559hg38UCSC Ensembl
chr1:194771333..194849689hg19UCSC Ensembl
chr1:193037956..193116312hg18UCSC Ensembl
Cytoband1q31.3
Allele length
AssemblyAllele length
hg3878357
hg1978357
hg1878357
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv548697, nsv548700
Samples1780862176_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv726n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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