A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv573744



Internal ID16014467
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:89738447..89915950hg38UCSC Ensembl
Innerchr16:89804855..89982358hg19UCSC Ensembl
Innerchr16:88332356..88509859hg18UCSC Ensembl
Cytoband16q24.3
Allele length
AssemblyAllele length
hg38177504
hg19177504
hg18177504
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149668
SamplesNINDS_233
Known GenesFANCA, SPIRE2, TCF25, ZNF276
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv573744
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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