A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6710n100



Internal ID22792797
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:143728285..143850167hg38UCSC Ensembl
chr7:143425378..143547260hg19UCSC Ensembl
chr7:143056311..143178193hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38121883
hg19121883
hg18121883
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1025246, nsv1030410, nsv1018110, nsv1020060, nsv1029574
Samples
Known GenesCTAGE6, FAM115C, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6710n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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