A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622400



Internal ID6662570
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:13233313..13234286hg38UCSC Ensembl
Innerchr10:13233319..13234280hg38UCSC Ensembl
Outerchr10:13233307..13234292hg38UCSC Ensembl
chr10:13275313..13276286hg19UCSC Ensembl
Innerchr10:13275319..13276280hg19UCSC Ensembl
Outerchr10:13275307..13276292hg19UCSC Ensembl
Cytoband10p13
Allele length
AssemblyAllele length
hg38974
hg19974
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13700159, essv13700161, essv13700165, essv13700163, essv13700160, essv13700162, essv13700164, essv13700166, essv13700167, essv13700168, essv13700169
SamplesHG03559, NA18504, NA19171, HG02885, HG02571, HG01879, HG02613, NA19440, HG03461, HG03539, HG02771
Known GenesUCMA
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622400
Frequency
Sample Size2504
Observed Gain0
Observed Loss11
Observed Complex0
Frequencyn/a


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