A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv582252



Internal ID16369661
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:77049075..77118365hg38UCSC Ensembl
Innerchr2:77276201..77345491hg19UCSC Ensembl
Innerchr2:77129709..77198999hg18UCSC Ensembl
Cytoband2p12
Allele length
AssemblyAllele length
hg3869291
hg1969291
hg1869291
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150234
Samples1780862355_A
Known GenesLRRTM4
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv582252
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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