A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv575949



Internal ID16363358
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:71187813..71236942hg38UCSC Ensembl
Innerchr17:69183954..69233083hg19UCSC Ensembl
Innerchr17:66695549..66744678hg18UCSC Ensembl
Cytoband17q24.3
Allele length
AssemblyAllele length
hg3849130
hg1949130
hg1849130
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv875926
Samples
Known GenesCASC17
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv575949
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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