A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574272



Internal ID16014995
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:4530305..4571949hg38UCSC Ensembl
Innerchr17:4433600..4475244hg19UCSC Ensembl
Innerchr17:4380349..4421993hg18UCSC Ensembl
Cytoband17p13.2
Allele length
AssemblyAllele length
hg3841645
hg1941645
hg1841645
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv866559, nssv866560
Samples
Known GenesGGT6, MYBBP1A, SPNS2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574272
Frequency
Sample Size17421
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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