A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614971



Internal ID7001860
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:128496890..128499655hg38UCSC Ensembl
Innerchr7:128496914..128499631hg38UCSC Ensembl
Outerchr7:128496866..128499679hg38UCSC Ensembl
chr7:128136944..128139709hg19UCSC Ensembl
Innerchr7:128136968..128139685hg19UCSC Ensembl
Outerchr7:128136920..128139733hg19UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg382766
hg192766
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12964810, essv12964809
SamplesHG02035, NA18533
Known GenesMETTL2B
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614971
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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