A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1012323



Internal ID18754856
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:16931436..16956580hg38UCSC Ensembl
Innerchr1:17257931..17283075hg19UCSC Ensembl
Innerchr1:17130518..17155662hg18UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3825145
hg1925145
hg1825145
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv127n100
Supporting Variantsnssv3474355
Samples
Known GenesCROCC
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1012323
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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