A curated catalogue of human genomic structural variation




Variant Details

Variant: dgv7656n100



Internal ID22793743
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:64462496..64886202hg38UCSC Ensembl
chr9:69474914..69898620hg19UCSC Ensembl
chr9:68764734..69188440hg18UCSC Ensembl
Cytoband9q12
Allele length
AssemblyAllele length
hg38423707
hg19423707
hg18423707
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnsv1023603, nsv1015599, nsv1021051
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)dgv7656n100
Frequency
Sample Size11257
Observed Gain3
Observed Loss4
Observed Complex0
Frequencyn/a


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