A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3601526



Internal ID6988563
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr4:97776680..97905560hg38UCSC Ensembl
Innerchr4:97776708..97905533hg38UCSC Ensembl
Outerchr4:97776653..97905588hg38UCSC Ensembl
chr4:98697831..98826711hg19UCSC Ensembl
Innerchr4:98697859..98826684hg19UCSC Ensembl
Outerchr4:98697804..98826739hg19UCSC Ensembl
Cytoband4q22.3
Allele length
AssemblyAllele length
hg38128881
hg19128881
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv11541556, essv11541558, essv11541557, essv11541559, essv11541555
SamplesHG01134, HG01435, HG01142, HG03949, HG01260
Known GenesSTPG2
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3601526
Frequency
Sample Size2504
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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