A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6459n100



Internal ID20158075
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:72523219..72853910hg38UCSC Ensembl
chr7:71988204..72324490hg19UCSC Ensembl
chr7:71626140..71962426hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38330692
hg19336287
hg18336287
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1030031, nsv1033946, nsv1017357, nsv1023444, nsv1026005, nsv1033080
Samples
Known GenesMIR4650-1, MIR4650-2, SBDSP1, TYW1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6459n100
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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