A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1062555



Internal ID18805086
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:9093317..9110590hg38UCSC Ensembl
Innerchr17:8996634..9013907hg19UCSC Ensembl
Innerchr17:8937359..8954632hg18UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg3817274
hg1917274
hg1817274
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3560340
Samples
Known GenesNTN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1062555
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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