A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12576155



Internal ID3891406
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:144326074..144333786hg38UCSC Ensembl
Innerchr6:144326107..144333754hg38UCSC Ensembl
Outerchr6:144326042..144333819hg38UCSC Ensembl
chr6:144647210..144654922hg19UCSC Ensembl
Innerchr6:144647243..144654890hg19UCSC Ensembl
Outerchr6:144647178..144654955hg19UCSC Ensembl
Cytoband6q24.2
Allele length
AssemblyAllele length
hg387713
hg197713
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3611106
Supporting Variants
SamplesHG03547
Known GenesUTRN
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12576155
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