A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6987590



Internal ID12630247
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr9:6695470..6902540hg38UCSC Ensembl
Innerchr9:6695470..6902540hg19UCSC Ensembl
Innerchr9:6685470..6892540hg18UCSC Ensembl
Innerchr9:6685470..6892540hg17UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg38207071
hg19207071
hg18207071
hg17207071
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752309
Supporting Variants
SamplesBEC_703
Known GenesKDM4C
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6987590
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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