A curated catalogue of human genomic structural variation




Variant Details

Variant: essv11038150



Internal ID6377084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:70007261..70016356hg38UCSC Ensembl
Innerchr3:70007411..70016206hg38UCSC Ensembl
Outerchr3:70007111..70016506hg38UCSC Ensembl
chr3:70056412..70065507hg19UCSC Ensembl
Innerchr3:70056562..70065357hg19UCSC Ensembl
Outerchr3:70056262..70065657hg19UCSC Ensembl
Cytoband3p13
Allele length
AssemblyAllele length
hg389096
hg199096
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3596507
Supporting Variants
SamplesNA20318
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv11038150
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