A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv562607



Internal ID16350016
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr13:85290164..85498872hg38UCSC Ensembl
Innerchr13:85864299..86073007hg19UCSC Ensembl
Innerchr13:84762300..84971008hg18UCSC Ensembl
Cytoband13q31.1
Allele length
AssemblyAllele length
hg38208709
hg19208709
hg18208709
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1148662
SamplesNINDS_182
Known GenesLINC00351
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv562607
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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