A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv581686



Internal ID16369095
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr2:44240247..44240905hg38UCSC Ensembl
Innerchr2:44467386..44468044hg19UCSC Ensembl
Innerchr2:44320890..44321548hg18UCSC Ensembl
Cytoband2p21
Allele length
AssemblyAllele length
hg38659
hg19659
hg18659
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6835n54
Supporting Variantsnssv907962, nssv907969, nssv907972, nssv907965, nssv907970, nssv907967, nssv907957, nssv907971, nssv907976, nssv907978, nssv907958, nssv907977, nssv907979, nssv907975, nssv907974, nssv907959, nssv907973, nssv907963, nssv907966, nssv907961, nssv907964, nssv907960, nssv907968, nssv907956
Samples
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv581686
Frequency
Sample Size17421
Observed Gain0
Observed Loss24
Observed Complex0
Frequencyn/a


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