A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515794



Internal ID15442851
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr1:47709195..47712255hg38UCSC Ensembl
Innerchr1:48174867..48177927hg19UCSC Ensembl
Innerchr1:47947454..47950514hg18UCSC Ensembl
Innerchr1:47886887..47889947hg17UCSC Ensembl
Cytoband1p33
Allele length
AssemblyAllele length
hg383061
hg193061
hg183061
hg173061
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv660050, nssv673299, nssv690119, nssv661894, nssv662898, nssv694006, nssv680790, nssv664814, nssv662482, nssv691966, nssv691214
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515794
Frequency
Sample Size2026
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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