A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3595648



Internal ID6635922
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:26637948..26649596hg38UCSC Ensembl
Innerchr3:26637975..26649570hg38UCSC Ensembl
Outerchr3:26637922..26649623hg38UCSC Ensembl
chr3:26679439..26691087hg19UCSC Ensembl
Innerchr3:26679466..26691061hg19UCSC Ensembl
Outerchr3:26679413..26691114hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg3811649
hg1911649
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv10960934
SamplesHG02798
Known GenesLRRC3B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3595648
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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