A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv584745



Internal ID16025468
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:237645391..237650474hg38UCSC Ensembl
Innerchr2:238554034..238559117hg19UCSC Ensembl
Innerchr2:238218773..238223856hg18UCSC Ensembl
Cytoband2q37.3
Allele length
AssemblyAllele length
hg385084
hg195084
hg185084
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv7347n54
Supporting Variantsnssv933698, nssv933688, nssv933687, nssv933693, nssv933695, nssv933686, nssv933696, nssv933690, nssv933692, nssv933691, nssv933694, nssv933697, nssv933689
Samples
Known GenesLRRFIP1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv584745
Frequency
Sample Size17421
Observed Gain0
Observed Loss13
Observed Complex0
Frequencyn/a


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