A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv524734



Internal ID15452027
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr19:56550704..56552271hg38UCSC Ensembl
Innerchr19:57062073..57063640hg19UCSC Ensembl
Innerchr19:61753885..61755452hg18UCSC Ensembl
Innerchr19:61753885..61755452hg17UCSC Ensembl
Cytoband19q13.43
Allele length
AssemblyAllele length
hg381568
hg191568
hg181568
hg171568
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv700725
Samples
Known GenesZFP28
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv524734
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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