A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613710



Internal ID6653919
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:74495098..74520125hg38UCSC Ensembl
Innerchr7:74495098..74520125hg38UCSC Ensembl
Outerchr7:74494598..74520625hg38UCSC Ensembl
chr7:73909428..73934455hg19UCSC Ensembl
Innerchr7:73909428..73934455hg19UCSC Ensembl
Outerchr7:73908928..73934955hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg3825028
hg1925028
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12845463
SamplesHG00342
Known GenesGTF2IRD1
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613710
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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