A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585333



Internal ID6625652
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:16215525..16244538hg38UCSC Ensembl
Innerchr1:16215548..16244515hg38UCSC Ensembl
Outerchr1:16215502..16244561hg38UCSC Ensembl
chr1:16542020..16571033hg19UCSC Ensembl
Innerchr1:16542043..16571010hg19UCSC Ensembl
Outerchr1:16541997..16571056hg19UCSC Ensembl
Cytoband1p36.13
Allele length
AssemblyAllele length
hg3829014
hg1929014
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9865048
SamplesHG03643
Known GenesRSG1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585333
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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