A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3613631



Internal ID6653840
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:71496000..71497848hg38UCSC Ensembl
Innerchr7:71496014..71497834hg38UCSC Ensembl
Outerchr7:71495986..71497862hg38UCSC Ensembl
chr7:70960985..70962833hg19UCSC Ensembl
Innerchr7:70960999..70962819hg19UCSC Ensembl
Outerchr7:70960971..70962847hg19UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg381849
hg191849
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv12829712
SamplesHG02035
Known GenesWBSCR17
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3613631
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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