A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699089



Internal ID15435741
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111333988..111343293hg38UCSC Ensembl
Innerchr7:110974044..110983349hg19UCSC Ensembl
Innerchr7:110761280..110770585hg18UCSC Ensembl
Innerchr7:110567995..110577300hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg389306
hg199306
hg189306
hg179306
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517394
Supporting Variants
Samples
Known GenesIMMP2L
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699089
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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