A curated catalogue of human genomic structural variation




Variant Details

Variant: essv12924161



Internal ID898747
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:109654635..109754537hg38UCSC Ensembl
Innerchr7:109654635..109754537hg38UCSC Ensembl
Outerchr7:109654135..109755037hg38UCSC Ensembl
chr7:109294692..109394594hg19UCSC Ensembl
Innerchr7:109294692..109394594hg19UCSC Ensembl
Outerchr7:109294192..109395094hg19UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3899903
hg1999903
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3614505
Supporting Variants
SamplesHG00524
Known Genes
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)essv12924161
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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