A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3638783



Internal ID7025568
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:61701490..61708625hg38UCSC Ensembl
Innerchr16:61701490..61708625hg38UCSC Ensembl
Outerchr16:61700990..61709125hg38UCSC Ensembl
chr16:61735394..61742529hg19UCSC Ensembl
Innerchr16:61735394..61742529hg19UCSC Ensembl
Outerchr16:61734894..61743029hg19UCSC Ensembl
Cytoband16q21
Allele length
AssemblyAllele length
hg387136
hg197136
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15496294
SamplesNA20340
Known GenesCDH8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3638783
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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