A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608135



Internal ID6995065
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:13702205..13705185hg38UCSC Ensembl
Innerchr6:13702252..13705139hg38UCSC Ensembl
Outerchr6:13702159..13705232hg38UCSC Ensembl
chr6:13702437..13705417hg19UCSC Ensembl
Innerchr6:13702484..13705371hg19UCSC Ensembl
Outerchr6:13702391..13705464hg19UCSC Ensembl
Cytoband6p23
Allele length
AssemblyAllele length
hg382981
hg192981
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12194168
SamplesNA19346
Known GenesRANBP9
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608135
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