A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6772n100



Internal ID20158388
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:158645675..159162536hg38UCSC Ensembl
chr7:158438367..158955227hg19UCSC Ensembl
chr7:158131128..158647988hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38516862
hg19516861
hg18516861
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033545, nsv1033355
Samples
Known GenesESYT2, LINC00689, NCAPG2, VIPR2, WDR60
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6772n100
Frequency
Sample Size29084
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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