A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6602n100



Internal ID22792689
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:122093318..122160326hg38UCSC Ensembl
chr7:121733372..121800380hg19UCSC Ensembl
chr7:121520608..121587616hg18UCSC Ensembl
Cytoband7q31.32
Allele length
AssemblyAllele length
hg3867009
hg1967009
hg1867009
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1034553, nsv1019004
Samples
Known GenesAASS
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6602n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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