A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607877



Internal ID6994808
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:1000670..1020400hg38UCSC Ensembl
Innerchr6:1000670..1020400hg38UCSC Ensembl
Outerchr6:1000170..1020900hg38UCSC Ensembl
chr6:1000905..1020635hg19UCSC Ensembl
Innerchr6:1000905..1020635hg19UCSC Ensembl
Outerchr6:1000405..1021135hg19UCSC Ensembl
Cytoband6p25.3
Allele length
AssemblyAllele length
hg3819731
hg1919731
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12172050
SamplesHG03917
Known GenesLOC285768
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607877
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