A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985210



Internal ID12982953
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111147914..111473535hg38UCSC Ensembl
Innerchr7:110787970..111113591hg19UCSC Ensembl
Innerchr7:110575206..110900827hg18UCSC Ensembl
Innerchr7:110381921..110707542hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38325622
hg19325622
hg18325622
hg17325622
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2752141
Supporting Variants
SamplesSPC_124
Known GenesIMMP2L
MethodSNP array
Analysis
PlatformAffymetrix Mapping 250K Nsp SNP Array
Comments
ReferencePinto_et_al_2007
Pubmed ID17911159
Accession Number(s)essv6985210
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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