A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575652



Internal ID16363061
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:54121732..54217655hg38UCSC Ensembl
Innerchr17:52199093..52295016hg19UCSC Ensembl
Innerchr17:49554092..49650015hg18UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg3895924
hg1995924
hg1895924
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1150564
Samples1780854496_A
Known GenesMIR548AJ2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575652
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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