A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6981186



Internal ID12626267
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:62642972..63840872hg38UCSC Ensembl
Innerchr7:62103350..63301250hg19UCSC Ensembl
Innerchr7:61740785..62938685hg18UCSC Ensembl
Innerchr7:61547500..62745400hg17UCSC Ensembl
Cytoband7q11.21
Allele length
AssemblyAllele length
hg381197901
hg191197901
hg181197901
hg171197901
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752164
Supporting Variants
SamplesBEC_361
Known GenesLOC100287704, LOC100287834, MIR4283-1, MIR4283-2, ZNF733P
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6981186
Frequency
Sample Size771
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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