A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv700425



Internal ID15090391
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:28957328..28959047hg38UCSC Ensembl
Innerchr7:28996944..28998663hg19UCSC Ensembl
Innerchr7:28963469..28965188hg18UCSC Ensembl
Innerchr7:28770184..28771903hg17UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg381720
hg191720
hg181720
hg171720
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv524487
Supporting Variants
Samples
Known GenesTRIL
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv700425
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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