A curated catalogue of human genomic structural variation




Variant Details

Variant: esv3614946



Internal ID7001835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:126991347..127044631hg38UCSC Ensembl
chr7:126631401..126684685hg19UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3853285
hg1953285
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv1329e214
Supporting Variantsessv12958301, essv12958302
SamplesNA20792, HG03727
Known GenesGRM8
MethodSequencing
Analysis
PlatformMultiple platforms
Comments
Reference1000_Genomes_Consortium_Phase_3
Pubmed ID21293372
Accession Number(s)esv3614946
Frequency
Sample Size2504
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer