A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9863645



Internal ID6488938
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3585311
Supporting Variants
SamplesHG01134
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv9863645
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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