A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6435n100



Internal ID22792522
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:65105195..65719808hg38UCSC Ensembl
chr7:64565573..65184781hg19UCSC Ensembl
chr7:64203008..64822216hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38614614
hg19619209
hg18619209
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028710, nsv1018486, nsv1028626, nsv1019070, nsv1021867, nsv1018265, nsv1015764, nsv1016478, nsv1018590, nsv1020690, nsv1021410, nsv1027826, nsv1032262, nsv1015680, nsv1015653
Samples
Known GenesINTS4L2, LOC441242, ZNF92
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6435n100
Frequency
Sample Size11257
Observed Gain0
Observed Loss22
Observed Complex0
Frequencyn/a


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