A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3608375



Internal ID6648614
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:24957513..24970781hg38UCSC Ensembl
Innerchr6:24957540..24970755hg38UCSC Ensembl
Outerchr6:24957487..24970808hg38UCSC Ensembl
chr6:24957741..24971009hg19UCSC Ensembl
Innerchr6:24957768..24970983hg19UCSC Ensembl
Outerchr6:24957715..24971036hg19UCSC Ensembl
Cytoband6p22.3
Allele length
AssemblyAllele length
hg3813269
hg1913269
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12231948, essv12231947, essv12231950, essv12231949
SamplesNA21123, NA20853, HG03823, HG03908
Known GenesFAM65B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3608375
Frequency
Sample Size2504
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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