A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv516541



Internal ID15097148
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:152404234..152417976hg38UCSC Ensembl
Innerchr1:152376710..152390452hg19UCSC Ensembl
Innerchr1:150643334..150657076hg18UCSC Ensembl
Innerchr1:149189783..149203525hg17UCSC Ensembl
Cytoband1q21.3
Allele length
AssemblyAllele length
hg3813743
hg1913743
hg1813743
hg1713743
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv672545, nssv669003
Samples
Known GenesCRNN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv516541
Frequency
Sample Size2026
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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