A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv679907



Internal ID15416559
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:103634120..103642774hg38UCSC Ensembl
Innerchr7:103274567..103283221hg19UCSC Ensembl
Innerchr7:103061803..103070457hg18UCSC Ensembl
Innerchr7:102868518..102877172hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg388655
hg198655
hg188655
hg178655
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516122
Supporting Variants
Samples
Known GenesRELN
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv679907
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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