A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3637598



Internal ID7024389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr16:921297..922718hg38UCSC Ensembl
Innerchr16:921326..922690hg38UCSC Ensembl
Outerchr16:921269..922747hg38UCSC Ensembl
chr16:971297..972718hg19UCSC Ensembl
Innerchr16:971326..972690hg19UCSC Ensembl
Outerchr16:971269..972747hg19UCSC Ensembl
Cytoband16p13.3
Allele length
AssemblyAllele length
hg381422
hg191422
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15357238
SamplesHG03388
Known GenesLMF1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3637598
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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