A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7525n100



Internal ID20159141
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:38989369..39342816hg38UCSC Ensembl
chr9:38989366..39342813hg19UCSC Ensembl
chr9:38979366..39332813hg18UCSC Ensembl
Cytoband9p13.1
Allele length
AssemblyAllele length
hg38353448
hg19353448
hg18353448
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033547, nsv1027420
Samples
Known GenesCNTNAP3
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7525n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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