A curated catalogue of human genomic structural variation




Variant Details

Variant: essv9740252



Internal ID18367812
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:38273366..38329399hg38UCSC Ensembl
Outerchr7:38253400..38344310hg38UCSC Ensembl
Innerchr7:38312967..38369000hg19UCSC Ensembl
Outerchr7:38293001..38383911hg19UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3890911
hg1990911
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv3541505
Supporting Variants
Samples
Known GenesTARP, TRG-AS1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceBoomsma_et_al_2014
Pubmed ID23714750
Accession Number(s)essv9740252
Frequency
Sample Size767
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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