A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3611328



Internal ID6998237
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr6:154742327..154748671hg38UCSC Ensembl
Innerchr6:154742327..154748671hg38UCSC Ensembl
Outerchr6:154742161..154748951hg38UCSC Ensembl
chr6:155063461..155069805hg19UCSC Ensembl
Innerchr6:155063461..155069805hg19UCSC Ensembl
Outerchr6:155063295..155070085hg19UCSC Ensembl
Cytoband6q25.2
Allele length
AssemblyAllele length
hg386345
hg196345
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12594531, essv12594532
SamplesHG02888, HG02586
Known GenesSCAF8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3611328
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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