A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636741



Internal ID7023535
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:64705399..64715563hg38UCSC Ensembl
Innerchr15:64705899..64715063hg38UCSC Ensembl
Outerchr15:64704399..64716563hg38UCSC Ensembl
chr15:64997598..65007762hg19UCSC Ensembl
Innerchr15:64998098..65007262hg19UCSC Ensembl
Outerchr15:64996598..65008762hg19UCSC Ensembl
Cytoband15q22.31
Allele length
AssemblyAllele length
hg3810165
hg1910165
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15271644, essv15271655, essv15271659, essv15271658, essv15271654, essv15271650, essv15271646, essv15271647, essv15271652, essv15271657, essv15271653, essv15271645, essv15271660, essv15271648, essv15271649, essv15271651, essv15271656
SamplesHG03096, HG03559, HG03175, HG03280, HG01140, HG03074, NA18519, NA19201, NA20287, HG03079, NA19159, HG01880, NA18856, HG01182, NA19225, NA19834, HG03166
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636741
Frequency
Sample Size2504
Observed Gain0
Observed Loss17
Observed Complex0
Frequencyn/a


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