A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3609786



Internal ID6996706
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:83947389..83947925hg38UCSC Ensembl
Innerchr6:83947398..83947916hg38UCSC Ensembl
Outerchr6:83947380..83947934hg38UCSC Ensembl
chr6:84657108..84657644hg19UCSC Ensembl
Innerchr6:84657117..84657635hg19UCSC Ensembl
Outerchr6:84657099..84657653hg19UCSC Ensembl
Cytoband6q14.2
Allele length
AssemblyAllele length
hg38537
hg19537
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12454079
SamplesHG02355
Known GenesCYB5R4
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3609786
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