A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12926387



Internal ID2928203
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 StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614532
Supporting Variants
SamplesHG03778
Known GenesIMMP2L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12926387
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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