A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv695828



Internal ID15432480
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:103634570..103642774hg38UCSC Ensembl
Innerchr7:103275017..103283221hg19UCSC Ensembl
Innerchr7:103062253..103070457hg18UCSC Ensembl
Innerchr7:102868968..102877172hg17UCSC Ensembl
Cytoband7q22.1
Allele length
AssemblyAllele length
hg388205
hg198205
hg188205
hg178205
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)nssv695828
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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