A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613929



Internal ID7000824
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:83231184..83288496hg38UCSC Ensembl
Innerchr7:83231197..83288483hg38UCSC Ensembl
Outerchr7:83231171..83288509hg38UCSC Ensembl
chr7:82860500..82917812hg19UCSC Ensembl
Innerchr7:82860513..82917799hg19UCSC Ensembl
Outerchr7:82860487..82917825hg19UCSC Ensembl
Cytoband7q21.11
Allele length
AssemblyAllele length
hg3857313
hg1957313
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12872245
SamplesHG00345
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613929
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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