A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608015



Internal ID6994946
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:7756286..7767198hg38UCSC Ensembl
Innerchr6:7756312..7767173hg38UCSC Ensembl
Outerchr6:7756261..7767224hg38UCSC Ensembl
chr6:7756519..7767431hg19UCSC Ensembl
Innerchr6:7756545..7767406hg19UCSC Ensembl
Outerchr6:7756494..7767457hg19UCSC Ensembl
Cytoband6p24.3
Allele length
AssemblyAllele length
hg3810913
hg1910913
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12182938
SamplesNA19083
Known GenesBMP6
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608015
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