A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10964590



Internal ID6567684
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:28421414..28431114hg38UCSC Ensembl
Innerchr3:28421458..28431071hg38UCSC Ensembl
Outerchr3:28421371..28431158hg38UCSC Ensembl
chr3:28462905..28472605hg19UCSC Ensembl
Innerchr3:28462949..28472562hg19UCSC Ensembl
Outerchr3:28462862..28472649hg19UCSC Ensembl
Cytoband3p24.1
Allele length
AssemblyAllele length
hg389701
hg199701
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595688
Supporting Variants
SamplesNA20759
Known GenesZCWPW2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10964590
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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