A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615339



Internal ID7002228
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:145304374..145321687hg38UCSC Ensembl
Innerchr7:145304374..145321687hg38UCSC Ensembl
Outerchr7:145303874..145322187hg38UCSC Ensembl
chr7:145001467..145018780hg19UCSC Ensembl
Innerchr7:145001467..145018780hg19UCSC Ensembl
Outerchr7:145000967..145019280hg19UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3817314
hg1917314
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12995852
SamplesHG01334
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615339
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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