A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv11624n54



Internal ID22779519
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:140175698..140177127hg38UCSC Ensembl
chr7:139875498..139876927hg19UCSC Ensembl
chr7:139521967..139523396hg18UCSC Ensembl
Cytoband7q34
Allele length
AssemblyAllele length
hg381430
hg191430
hg181430
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv608493, nsv608485, nsv608494, nsv608495, nsv608489
Samples
Known GenesKDM7A
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)dgv11624n54
Frequency
Sample Size17421
Observed Gain6
Observed Loss0
Observed Complex0
Frequencyn/a


Hosted by The Centre for Applied Genomics
Grant support for DGV
Please read the usage disclaimer