A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3622726



Internal ID6662895
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr10:27505039..27506955hg38UCSC Ensembl
Innerchr10:27505044..27506950hg38UCSC Ensembl
Outerchr10:27505034..27506960hg38UCSC Ensembl
chr10:27793968..27795884hg19UCSC Ensembl
Innerchr10:27793973..27795879hg19UCSC Ensembl
Outerchr10:27793963..27795889hg19UCSC Ensembl
Cytoband10p12.1
Allele length
AssemblyAllele length
hg381917
hg191917
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13733565, essv13733570, essv13733566, essv13733569, essv13733558, essv13733579, essv13733573, essv13733564, essv13733578, essv13733560, essv13733567, essv13733568, essv13733576, essv13733575, essv13733577, essv13733559, essv13733574, essv13733563, essv13733562, essv13733572, essv13733571, essv13733561
SamplesHG01811, HG01852, HG01849, HG02048, NA18591, HG00581, NA18963, HG00557, HG01843, HG00692, HG01851, HG00451, HG01797, HG01874, HG02127, HG04161, NA18986, HG00458, HG02072, NA19063, HG02522, HG01869
Known GenesRAB18
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3622726
Frequency
Sample Size2504
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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