A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1006860



Internal ID18749391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16518425..16641627hg38UCSC Ensembl
Innerchr1:16844920..16968122hg19UCSC Ensembl
Innerchr1:16717507..16840709hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg38123203
hg19123203
hg18123203
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv43n100
Supporting Variantsnssv3698793
Samples
Known GenesCROCCP2, MIR3675, NBPF1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1006860
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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