A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv657n54



Internal ID22768552
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:180781345..180786185hg38UCSC Ensembl
chr1:180750481..180755321hg19UCSC Ensembl
chr1:179017104..179021944hg18UCSC Ensembl
Cytoband1q25.3
Allele length
AssemblyAllele length
hg384841
hg194841
hg184841
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv548354, nsv548351, nsv548350, nsv548353, nsv548347, nsv548349, nsv548348, nsv548352
Samples
Known GenesXPR1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv657n54
Frequency
Sample Size17421
Observed Gain0
Observed Loss36
Observed Complex0
Frequencyn/a


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