A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3469861



Internal ID18716919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16559628..16627335hg38UCSC Ensembl
Innerchr1:16886123..16953830hg19UCSC Ensembl
Innerchr1:16758710..16826417hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3867708
hg1967708
hg1867708
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1004437
Supporting Variants
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)nssv3469861
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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