A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv671727



Internal ID15061693
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:129752029..129777890hg38UCSC Ensembl
Innerchr7:129391869..129417730hg19UCSC Ensembl
Innerchr7:129179105..129204966hg18UCSC Ensembl
Innerchr7:128985820..129011681hg17UCSC Ensembl
Cytoband7q32.2
Allele length
AssemblyAllele length
hg3825862
hg1925862
hg1825862
hg1725862
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516024
Supporting Variants
Samples
Known GenesMIR182, MIR183, MIR96, NRF1
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv671727
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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