A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv545618



Internal ID15986341
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:15749411..15799712hg38UCSC Ensembl
Innerchr1:16075906..16126207hg19UCSC Ensembl
Innerchr1:15948493..15998794hg18UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg3850302
hg1950302
hg1850302
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1173777
SamplesNINDS_70
Known GenesFBLIM1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv545618
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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