A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv691686



Internal ID15428338
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111333988..111676384hg38UCSC Ensembl
Innerchr7:110974044..111316440hg19UCSC Ensembl
Innerchr7:110761280..111103676hg18UCSC Ensembl
Innerchr7:110567995..110910391hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38342397
hg19342397
hg18342397
hg17342397
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)nssv691686
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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