A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1003309



Internal ID19092528
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:67930106..68013406hg38UCSC Ensembl
Innerchr2:68157238..68240538hg19UCSC Ensembl
Innerchr2:68010742..68094042hg18UCSC Ensembl
Cytoband2p14
Allele length
AssemblyAllele length
hg3883301
hg1983301
hg1883301
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3730860
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)nsv1003309
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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