A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7657n100



Internal ID22793744
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64462496..64954062hg38UCSC Ensembl
chr9:69474914..69966480hg19UCSC Ensembl
chr9:68764734..69256300hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38491567
hg19491567
hg18491567
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1032179, nsv1015962, nsv1026163, nsv1020650, nsv1018085, nsv1024881, nsv1026281
Samples
Known GenesLOC100133920
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)dgv7657n100
Frequency
Sample Size11257
Observed Gain9
Observed Loss0
Observed Complex0
Frequencyn/a


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