A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3598162



Internal ID6638427
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:150662799..150664566hg38UCSC Ensembl
Innerchr3:150662849..150664516hg38UCSC Ensembl
Outerchr3:150662749..150664616hg38UCSC Ensembl
chr3:150380586..150382353hg19UCSC Ensembl
Innerchr3:150380636..150382303hg19UCSC Ensembl
Outerchr3:150380536..150382403hg19UCSC Ensembl
Cytoband3q25.1
Allele length
AssemblyAllele length
hg381768
hg191768
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11181404
SamplesHG00232
Known GenesFAM194A
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3598162
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