A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6336n100



Internal ID22792423
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:38339117..38378864hg38UCSC Ensembl
chr7:38378718..38418465hg19UCSC Ensembl
chr7:38345243..38384990hg18UCSC Ensembl
Cytoband7p14.1
Allele length
AssemblyAllele length
hg3839748
hg1939748
hg1839748
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1016350, nsv1021462, nsv1032769, nsv1020630
Samples
Known GenesTRG-AS1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6336n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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