A curated catalogue of human genomic structural variation




Variant Details

Variant: essv10916338



Internal ID918154
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr3:7518416..7521160hg38UCSC Ensembl
Innerchr3:7518466..7521110hg38UCSC Ensembl
Outerchr3:7518366..7521210hg38UCSC Ensembl
chr3:7560103..7562847hg19UCSC Ensembl
Innerchr3:7560153..7562797hg19UCSC Ensembl
Outerchr3:7560053..7562897hg19UCSC Ensembl
Cytoband3p26.1
Allele length
AssemblyAllele length
hg382745
hg192745
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3595198
Supporting Variants
SamplesHG04186
Known GenesGRM7
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv10916338
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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