A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015014



Internal ID19104231
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:123486218..123566824hg38UCSC Ensembl
Innerchr2:124243794..124324400hg19UCSC Ensembl
Innerchr2:123960264..124040870hg18UCSC Ensembl
Cytoband2q14.3
Allele length
AssemblyAllele length
hg3880607
hg1980607
hg1880607
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3580710
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1015014
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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