A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6984840



Internal ID12983593
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:10758865..10914592hg38UCSC Ensembl
Innerchr7:10798492..10954219hg19UCSC Ensembl
Innerchr7:10765017..10920744hg18UCSC Ensembl
Innerchr7:10571732..10727459hg17UCSC Ensembl
Cytoband7p21.3
Allele length
AssemblyAllele length
hg38155728
hg19155728
hg18155728
hg17155728
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752139
Supporting Variants
SamplesSPC_183
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6984840
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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