A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565427



Internal ID16352836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:85388811..85429817hg38UCSC Ensembl
Innerchr14:85855155..85896161hg19UCSC Ensembl
Innerchr14:84924908..84965914hg18UCSC Ensembl
Cytoband14q31.3
Allele length
AssemblyAllele length
hg3841007
hg1941007
hg1841007
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149505, nssv831940
SamplesNINDS_172
Known GenesLINC00911
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565427
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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