A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585311



Internal ID6625631
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:15448170..15455268hg38UCSC Ensembl
Innerchr1:15448320..15455118hg38UCSC Ensembl
Outerchr1:15448020..15455418hg38UCSC Ensembl
chr1:15774665..15781763hg19UCSC Ensembl
Innerchr1:15774815..15781613hg19UCSC Ensembl
Outerchr1:15774515..15781913hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg387099
hg197099
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9863645
SamplesHG01134
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585311
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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