A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv549001



Internal ID15989724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:203094958..203096006hg38UCSC Ensembl
Innerchr1:203064086..203065134hg19UCSC Ensembl
Innerchr1:201330709..201331757hg18UCSC Ensembl
Cytoband1q32.1
Allele length
AssemblyAllele length
hg381049
hg191049
hg181049
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv734690, nssv734691
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv549001
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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