A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575948



Internal ID16363357
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:70946872..71014982hg38UCSC Ensembl
Innerchr17:68943013..69011123hg19UCSC Ensembl
Innerchr17:66454608..66522718hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3868111
hg1968111
hg1868111
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1149797
SamplesNINDS_174
Known Genes
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575948
Frequency
Sample Size17421
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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