A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047096



Internal ID19136315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:48444284..48496988hg38UCSC Ensembl
Innerchr14:48913487..48966191hg19UCSC Ensembl
Innerchr14:47983237..48035941hg18UCSC Ensembl
Cytoband14q21.3
Allele length
AssemblyAllele length
hg3852705
hg1952705
hg1852705
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3531007
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)nsv1047096
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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