A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3615426



Internal ID7002315
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:149096928..149105618hg38UCSC Ensembl
Innerchr7:149096928..149105618hg38UCSC Ensembl
Outerchr7:149096428..149106118hg38UCSC Ensembl
chr7:148794020..148802710hg19UCSC Ensembl
Innerchr7:148794020..148802710hg19UCSC Ensembl
Outerchr7:148793520..148803210hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg388691
hg198691
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv13003865
SamplesHG00280
Known GenesZNF425
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3615426
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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