A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985764



Internal ID12983991
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:16845236..16902835hg38UCSC Ensembl
Innerchr7:16884860..16942459hg19UCSC Ensembl
Innerchr7:16851385..16908984hg18UCSC Ensembl
Innerchr7:16658100..16715699hg17UCSC Ensembl
Cytoband7p21.1
Allele length
AssemblyAllele length
hg3857600
hg1957600
hg1857600
hg1757600
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752152
Supporting Variants
SamplesSPC_42
Known GenesAGR3
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Sty2 SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985764
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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