A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3623834



Internal ID6664001
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:74607810..74614792hg38UCSC Ensembl
Innerchr10:74607817..74614785hg38UCSC Ensembl
Outerchr10:74607803..74614799hg38UCSC Ensembl
chr10:76367568..76374550hg19UCSC Ensembl
Innerchr10:76367575..76374543hg19UCSC Ensembl
Outerchr10:76367561..76374557hg19UCSC Ensembl
Cytoband10q22.2
Allele length
AssemblyAllele length
hg386983
hg196983
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13863658, essv13863650, essv13863653, essv13863656, essv13863652, essv13863657, essv13863661, essv13863648, essv13863660, essv13863654, essv13863649, essv13863659, essv13863655, essv13863651
SamplesHG04210, HG02017, HG03490, HG03765, NA20795, HG03905, HG03884, NA12748, HG03643, NA18541, HG01444, NA20792, NA19785, HG01082
Known GenesADK
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3623834
Frequency
Sample Size2504
Observed Gain0
Observed Loss14
Observed Complex0
Frequencyn/a


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