A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6607n100



Internal ID22792694
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:124950634..125033319hg38UCSC Ensembl
chr7:124590688..124673373hg19UCSC Ensembl
chr7:124377924..124460609hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3882686
hg1982686
hg1882686
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1032336, nsv1034654, nsv1025873
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6607n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss4
Observed Complex0
Frequencyn/a


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