A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3636871



Internal ID6676978
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr15:72171228..72178664hg38UCSC Ensembl
Innerchr15:72171728..72178164hg38UCSC Ensembl
Outerchr15:72170228..72179664hg38UCSC Ensembl
chr15:72463569..72471005hg19UCSC Ensembl
Innerchr15:72464069..72470505hg19UCSC Ensembl
Outerchr15:72462569..72472005hg19UCSC Ensembl
Cytoband15q23
Allele length
AssemblyAllele length
hg387437
hg197437
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv15289537, essv15289538
SamplesNA20588, NA19917
Known GenesGRAMD2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3636871
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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