A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2669004



Internal ID9935109
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr16:14535631..14540706hg38UCSC Ensembl
Outerchr16:14535594..14540756hg38UCSC Ensembl
Innerchr16:14629488..14634563hg19UCSC Ensembl
Outerchr16:14629451..14634613hg19UCSC Ensembl
Cytoband16p13.12
Allele length
AssemblyAllele length
hg385163
hg195163
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6225521
SamplesNA19085
Known GenesPARN
MethodMerging
AnalysisNo reference, merging analysis
PlatformMerging
CommentsHigh quality site
Reference1000_Genomes_Consortium_Phase_1
Pubmed ID23128226
Accession Number(s)esv2669004
Frequency
Sample Size1151
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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