A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv572895



Internal ID16360304
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:64084865..64126827hg38UCSC Ensembl
Innerchr16:64118769..64160731hg19UCSC Ensembl
Innerchr16:62676270..62718232hg18UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg3841963
hg1941963
hg1841963
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv5177n54
Supporting Variantsnssv1149182
Samples1782681086_A
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv572895
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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