A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3585290



Internal ID6972815
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr1:14835122..14839178hg38UCSC Ensembl
Innerchr1:14835122..14839178hg38UCSC Ensembl
Outerchr1:14834984..14839262hg38UCSC Ensembl
chr1:15161618..15165674hg19UCSC Ensembl
Innerchr1:15161618..15165674hg19UCSC Ensembl
Outerchr1:15161480..15165758hg19UCSC Ensembl
Cytoband1p36.21
Allele length
AssemblyAllele length
hg384057
hg194057
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv9863413
SamplesHG01779
Known GenesKAZN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3585290
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer