A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613761



Internal ID7000656
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:76385488..76389357hg38UCSC Ensembl
Innerchr7:76385988..76388857hg38UCSC Ensembl
Outerchr7:76384488..76390357hg38UCSC Ensembl
chr7:76014805..76018674hg19UCSC Ensembl
Innerchr7:76015305..76018174hg19UCSC Ensembl
Outerchr7:76013805..76019674hg19UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg383870
hg193870
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12848881
SamplesNA12044
Known GenesSRCRB4D
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613761
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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