A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv669590



Internal ID15059556
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:227850423..228037123hg38UCSC Ensembl
Innerchr1:228038124..228224824hg19UCSC Ensembl
Innerchr1:226104747..226291447hg18UCSC Ensembl
Innerchr1:224344859..224531559hg17UCSC Ensembl
Cytoband1q42.13
Allele length
AssemblyAllele length
hg38186701
hg19186701
hg18186701
hg17186701
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516409
Supporting Variants
Samples
Known GenesMIR5008, WNT3A, WNT9A
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv669590
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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