A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6616n100



Internal ID22792703
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:131331684..131471005hg38UCSC Ensembl
chr7:131016443..131155764hg19UCSC Ensembl
chr7:130666983..130806304hg18UCSC Ensembl
Cytoband7q32.3
Allele length
AssemblyAllele length
hg38139322
hg19139322
hg18139322
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1033696, nsv1017991, nsv1027870
Samples
Known GenesMKLN1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6616n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss3
Observed Complex0
Frequencyn/a


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