A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3890822



Internal ID18838438
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:31819853..31827305hg38UCSC Ensembl
Outerchr6:31817451..31829645hg38UCSC Ensembl
Innerchr6:31787630..31795082hg19UCSC Ensembl
Outerchr6:31785228..31797422hg19UCSC Ensembl
Innerchr6:31895609..31903061hg18UCSC Ensembl
Outerchr6:31893207..31905401hg18UCSC Ensembl
Cytoband6p21.32
Allele length
AssemblyAllele length
hg3812195
hg1912195
hg1812195
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv25781232, essv25780722, essv25780532, essv25785674, essv25779350
Samples
Known GenesHSPA1A, HSPA1B
MethodSNP array
Analysis
PlatformIllumina HumanHap 610
Comments
ReferenceSuktitipat_et_al_2014
Pubmed ID25118596
Accession Number(s)esv3890822
Frequency
Sample Size3017
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer