A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv434n21



Internal ID18990907
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr7:147640650..147663725hg38UCSC Ensembl
chr7:147337742..147360817hg19UCSC Ensembl
chr7:146968675..146991750hg18UCSC Ensembl
chr7:146775390..146798465hg17UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg3823076
hg1923076
hg1823076
hg1723076
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv527018, nsv516942
Samples
Known GenesCNTNAP2
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)dgv434n21
Frequency
Sample Size2026
Observed Gain0
Observed Loss5
Observed Complex0
Frequencyn/a


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