A curated catalogue of human genomic structural variation




Variant Details

Variant: esv2752157



Internal ID12985709
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:4438361..4605758hg38UCSC Ensembl
Innerchr7:4477992..4645389hg19UCSC Ensembl
Innerchr7:4444518..4611915hg18UCSC Ensembl
Innerchr7:4251233..4418630hg17UCSC Ensembl
Cytoband7p22.1
Allele length
AssemblyAllele length
hg38167398
hg19167398
hg18167398
hg17167398
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsessv6987488, essv6984101, essv6984100
SamplesBEC_774
Known Genes
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
CommentsSample level SV from stringent call set
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)esv2752157
Frequency
Sample Size771
Observed Gain3
Observed Loss0
Observed Complex0
Frequencyn/a


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