A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613175



Internal ID7000073
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:52853261..52919284hg38UCSC Ensembl
Innerchr7:52853274..52919272hg38UCSC Ensembl
Outerchr7:52853249..52919297hg38UCSC Ensembl
chr7:52920954..52986977hg19UCSC Ensembl
Innerchr7:52920967..52986965hg19UCSC Ensembl
Outerchr7:52920942..52986990hg19UCSC Ensembl
Cytoband7p12.1
Allele length
AssemblyAllele length
hg3866024
hg1966024
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12777328
SamplesHG03025
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613175
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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