A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3587784



Internal ID6975207
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:164009376..164322309hg38UCSC Ensembl
Innerchr1:164009388..164322298hg38UCSC Ensembl
Outerchr1:164009365..164322321hg38UCSC Ensembl
chr1:163978613..164291546hg19UCSC Ensembl
Innerchr1:163978625..164291535hg19UCSC Ensembl
Outerchr1:163978602..164291558hg19UCSC Ensembl
Cytoband1q23.3
Allele length
AssemblyAllele length
hg38312934
hg19312934
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10174950
SamplesHG02085
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3587784
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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