A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608709



Internal ID6995633
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:36619569..36627172hg38UCSC Ensembl
Innerchr6:36619569..36627172hg38UCSC Ensembl
Outerchr6:36619360..36627360hg38UCSC Ensembl
chr6:36587346..36594949hg19UCSC Ensembl
Innerchr6:36587346..36594949hg19UCSC Ensembl
Outerchr6:36587137..36595137hg19UCSC Ensembl
Cytoband6p21.31
Allele length
AssemblyAllele length
hg387604
hg197604
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12320371
SamplesNA18986
Known GenesMIR3925
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608709
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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