A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1061446



Internal ID19150665
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:5547842..5590676hg38UCSC Ensembl
Innerchr17:5451162..5493996hg19UCSC Ensembl
Innerchr17:5391886..5434720hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3842835
hg1942835
hg1842835
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560134
Samples
Known GenesNLRP1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1061446
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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