A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6549n100



Internal ID22792636
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:108295461..108365594hg38UCSC Ensembl
chr7:107935905..108006038hg19UCSC Ensembl
chr7:107723141..107793274hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3870134
hg1970134
hg1870134
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1031824, nsv1019059, nsv1021783, nsv1017288
Samples
Known GenesNRCAM
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6549n100
Frequency
Sample Size11257
Observed Gain5
Observed Loss0
Observed Complex0
Frequencyn/a


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