A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3600231



Internal ID6987275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:36512165..36565428hg38UCSC Ensembl
Innerchr4:36512165..36565428hg38UCSC Ensembl
Outerchr4:36511665..36565928hg38UCSC Ensembl
chr4:36513787..36567050hg19UCSC Ensembl
Innerchr4:36513787..36567050hg19UCSC Ensembl
Outerchr4:36513287..36567550hg19UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg3853264
hg1953264
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11395353
SamplesNA18986
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3600231
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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