A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3530207



Internal ID18828488
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:42430859..42509860hg38UCSC Ensembl
Innerchr14:42900062..42979063hg19UCSC Ensembl
Innerchr14:41969812..42048813hg18UCSC Ensembl
Cytoband14q21.1
Allele length
AssemblyAllele length
hg3879002
hg1979002
hg1879002
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1051049
Supporting Variants
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)nssv3530207
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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