A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3607955



Internal ID6994886
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:4725918..4729538hg38UCSC Ensembl
Innerchr6:4725918..4729538hg38UCSC Ensembl
Outerchr6:4725699..4729840hg38UCSC Ensembl
chr6:4726152..4729772hg19UCSC Ensembl
Innerchr6:4726152..4729772hg19UCSC Ensembl
Outerchr6:4725933..4730074hg19UCSC Ensembl
Cytoband6p25.1
Allele length
AssemblyAllele length
hg383621
hg193621
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12179522, essv12179517, essv12179520, essv12179521, essv12179516, essv12179519, essv12179518
SamplesHG03559, HG02890, HG02536, HG02595, HG02887, HG03432, NA19102
Known GenesCDYL
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3607955
Frequency
Sample Size2504
Observed Gain0
Observed Loss7
Observed Complex0
Frequencyn/a


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