A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv708559



Internal ID15655829
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:1342153..1360773hg38UCSC Ensembl
Innerchr1:1277533..1296153hg19UCSC Ensembl
Innerchr1:1267396..1286016hg18UCSC Ensembl
Cytoband1p36.33
Allele length
AssemblyAllele length
hg3818621
hg1918621
hg1818621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv544991
Supporting Variants
Samples
Known GenesDVL1, MXRA8
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv708559
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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