A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1149505



Internal ID15880194
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 StatusS
Merged Variantsnsv565427
Supporting Variants
SamplesNINDS_172
Known GenesLINC00911
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1149505
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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