A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614532



Internal ID6654737
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:110697304..110736218hg38UCSC Ensembl
Innerchr7:110697304..110736218hg38UCSC Ensembl
Outerchr7:110697062..110736443hg38UCSC Ensembl
chr7:110337360..110376274hg19UCSC Ensembl
Innerchr7:110337360..110376274hg19UCSC Ensembl
Outerchr7:110337118..110376499hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3838915
hg1938915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12926387
SamplesHG03778
Known GenesIMMP2L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614532
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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