A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574427



Internal ID16361836
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:14999101..15012285hg38UCSC Ensembl
Innerchr17:14902418..14915602hg19UCSC Ensembl
Innerchr17:14843143..14856327hg18UCSC Ensembl
Cytoband17p12
Allele length
AssemblyAllele length
hg3813185
hg1913185
hg1813185
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149732
SamplesNINDS_132
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574427
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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