A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv565872



Internal ID16353281
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr14:101457695..101458698hg38UCSC Ensembl
Innerchr14:101924032..101925035hg19UCSC Ensembl
Innerchr14:100993785..100994788hg18UCSC Ensembl
Cytoband14q32.31
Allele length
AssemblyAllele length
hg381004
hg191004
hg181004
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv3916n54
Supporting Variantsnssv833706
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv565872
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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