A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv6411n100



Internal ID22792498
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:62506780..63299342hg38UCSC Ensembl
chr7:61875418..62759720hg19UCSC Ensembl
chr7:61512853..62397155hg18UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg38792563
hg19884303
hg18884303
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1028855, nsv1025546, nsv1034891, nsv1021114, nsv1025454, nsv1023449, nsv1033641, nsv1027594, nsv1020320, nsv1015314, nsv1028826, nsv1031344, nsv1034982, nsv1032212, nsv1033540, nsv1029240, nsv1022009, nsv1031758, nsv1028799, nsv1033292
Samples
Known GenesZNF733P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv6411n100
Frequency
Sample Size11257
Observed Gain34
Observed Loss0
Observed Complex0
Frequencyn/a


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