A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15426936



Internal ID4296957
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:23627203..23632845hg38UCSC Ensembl
Innerchr16:23627251..23632797hg38UCSC Ensembl
Outerchr16:23627155..23632893hg38UCSC Ensembl
chr16:23638524..23644166hg19UCSC Ensembl
Innerchr16:23638572..23644118hg19UCSC Ensembl
Outerchr16:23638476..23644214hg19UCSC Ensembl
Cytoband16p12.2
Allele length
AssemblyAllele length
hg385643
hg195643
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3638232
Supporting Variants
SamplesHG03857
Known GenesPALB2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15426936
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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