A curated catalogue of human genomic structural variation




Variant Details

Variant: essv15289538



Internal ID5291354
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3636871
Supporting Variants
SamplesNA20588
Known GenesGRAMD2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv15289538
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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