A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637620



Internal ID6677723
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1616557..1617485hg38UCSC Ensembl
Innerchr16:1616576..1617466hg38UCSC Ensembl
Outerchr16:1616538..1617504hg38UCSC Ensembl
chr16:1666558..1667486hg19UCSC Ensembl
Innerchr16:1666577..1667467hg19UCSC Ensembl
Outerchr16:1666539..1667505hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38929
hg19929
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15362325
SamplesHG02721
Known GenesCRAMP1L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637620
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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