A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636288



Internal ID7023084
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:43176675..43178191hg38UCSC Ensembl
Innerchr15:43176725..43178133hg38UCSC Ensembl
Outerchr15:43176598..43178268hg38UCSC Ensembl
chr15:43468873..43470389hg19UCSC Ensembl
Innerchr15:43468923..43470331hg19UCSC Ensembl
Outerchr15:43468796..43470466hg19UCSC Ensembl
Cytoband15q15.2
Allele length
AssemblyAllele length
hg381517
hg191517
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15231136, essv15231126, essv15231127, essv15231145, essv15231135, essv15231125, essv15231142, essv15231138, essv15231134, essv15231143, essv15231139, essv15231141, essv15231129, essv15231140, essv15231128, essv15231137, essv15231144, essv15231130, essv15231132, essv15231133, essv15231131
SamplesHG01985, HG02496, HG03121, NA18924, NA19332, HG02804, NA18878, NA19443, NA19457, NA19922, NA19200, NA19908, NA19984, HG03461, HG01375, NA20357, HG02970, HG03063, NA19900, HG02947, HG03129
Known GenesTMEM62
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636288
Frequency
Sample Size2504
Observed Gain0
Observed Loss21
Observed Complex0
Frequencyn/a


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