A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573413



Internal ID16014136
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:83990319..84002314hg38UCSC Ensembl
Innerchr16:84023924..84035919hg19UCSC Ensembl
Innerchr16:82581425..82593420hg18UCSC Ensembl
Cytoband16q23.3
Allele length
AssemblyAllele length
hg3811996
hg1911996
hg1811996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149327
Samples1798860361_A
Known GenesNECAB2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573413
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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