A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3528577



Internal ID18826858
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:28096481..28140455hg38UCSC Ensembl
Innerchr14:28565687..28609661hg19UCSC Ensembl
Innerchr14:27635438..27679412hg18UCSC Ensembl
Cytoband14q12
Allele length
AssemblyAllele length
hg3843975
hg1943975
hg1843975
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1039658
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)nssv3528577
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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