A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3612860



Internal ID6999759
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:37731290..37853637hg38UCSC Ensembl
chr7:37770892..37893239hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg38122348
hg19122348
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1281e214
Supporting Variantsessv12738673
SamplesNA19025
Known GenesGPR141, NME8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3612860
Frequency
Sample Size2504
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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