A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv997666



Internal ID18810516
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16559628..16637216hg38UCSC Ensembl
Innerchr1:16886123..16963711hg19UCSC Ensembl
Innerchr1:16758710..16836298hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3877589
hg1977589
hg1877589
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv56n100
Supporting Variantsnssv3464308
Samples
Known GenesCROCCP2, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv997666
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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