A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1037668



Internal ID18780199
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:20896061..20957189hg38UCSC Ensembl
Innerchr14:21364220..21425348hg19UCSC Ensembl
Innerchr14:20434060..20495188hg18UCSC Ensembl
Cytoband14q11.2
Allele length
AssemblyAllele length
hg3861129
hg1961129
hg1861129
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1802n100
Supporting Variantsnssv3712156
Samples
Known GenesECRP, RNASE2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1037668
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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