A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615051



Internal ID7001940
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131973006..131982383hg38UCSC Ensembl
Innerchr7:131973030..131982360hg38UCSC Ensembl
Outerchr7:131972983..131982407hg38UCSC Ensembl
chr7:131657765..131667142hg19UCSC Ensembl
Innerchr7:131657789..131667119hg19UCSC Ensembl
Outerchr7:131657742..131667166hg19UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg389378
hg199378
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12972732
SamplesHG03703
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615051
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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