A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637621



Internal ID6677724
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:1636879..1637608hg38UCSC Ensembl
Innerchr16:1636894..1637594hg38UCSC Ensembl
Outerchr16:1636865..1637623hg38UCSC Ensembl
chr16:1686880..1687609hg19UCSC Ensembl
Innerchr16:1686895..1687595hg19UCSC Ensembl
Outerchr16:1686866..1687624hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg38730
hg19730
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15362326
SamplesHG02131
Known GenesCRAMP1L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637621
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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