A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6985211



Internal ID12982954
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111279993..111415993hg38UCSC Ensembl
Innerchr7:110920049..111056049hg19UCSC Ensembl
Innerchr7:110707285..110843285hg18UCSC Ensembl
Innerchr7:110514000..110650000hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38136001
hg19136001
hg18136001
hg17136001
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)essv6985211
Frequency
Sample Size771
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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