A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv574580



Internal ID16015303
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:19717164..19760434hg38UCSC Ensembl
Innerchr17:19620477..19663747hg19UCSC Ensembl
Innerchr17:19561069..19604339hg18UCSC Ensembl
Cytoband17p11.2
Allele length
AssemblyAllele length
hg3843271
hg1943271
hg1843271
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149756
SamplesHGDP00961
Known GenesALDH3A1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv574580
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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