A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614528



Internal ID6654733
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:110676142..110683487hg38UCSC Ensembl
Innerchr7:110676183..110683446hg38UCSC Ensembl
Outerchr7:110676101..110683528hg38UCSC Ensembl
chr7:110316198..110323543hg19UCSC Ensembl
Innerchr7:110316239..110323502hg19UCSC Ensembl
Outerchr7:110316157..110323584hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg387346
hg197346
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12926382
SamplesHG02367
Known GenesIMMP2L
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614528
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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