A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1047924



Internal ID19137143
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85359936..85401884hg38UCSC Ensembl
Innerchr14:85826280..85868228hg19UCSC Ensembl
Innerchr14:84896033..84937981hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3841949
hg1941949
hg1841949
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3532366
Samples
Known GenesLINC00911
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1047924
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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