A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637636



Internal ID6677739
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:2737650..2739977hg38UCSC Ensembl
Innerchr16:2737651..2739976hg38UCSC Ensembl
Outerchr16:2737649..2739978hg38UCSC Ensembl
chr16:2787651..2789978hg19UCSC Ensembl
Innerchr16:2787652..2789977hg19UCSC Ensembl
Outerchr16:2787650..2789979hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg382328
hg192328
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15362808
SamplesNA18878
Known GenesSRRM2-AS1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637636
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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