A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv580388



Internal ID16367797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56620068..56691737hg38UCSC Ensembl
Innerchr19:57131436..57203105hg19UCSC Ensembl
Innerchr19:61823248..61894917hg18UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg3871670
hg1971670
hg1871670
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv901979
Samples
Known GenesSMIM17, ZNF71, ZNF835
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv580388
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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