A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699398



Internal ID15436050
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111383266..111408523hg38UCSC Ensembl
Innerchr7:111023322..111048579hg19UCSC Ensembl
Innerchr7:110810558..110835815hg18UCSC Ensembl
Innerchr7:110617273..110642530hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3825258
hg1925258
hg1825258
hg1725258
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)nssv699398
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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