A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv701554



Internal ID15438206
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr4:36607666..36614976hg38UCSC Ensembl
Innerchr4:36609288..36616598hg19UCSC Ensembl
Innerchr4:36285683..36292993hg18UCSC Ensembl
Innerchr4:36431854..36439164hg17UCSC Ensembl
Cytoband4p14
Allele length
AssemblyAllele length
hg387311
hg197311
hg187311
hg177311
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv525428
Supporting Variants
Samples
Known Genes
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv701554
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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