A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv699707



Internal ID15089673
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:93365966..93393908hg38UCSC Ensembl
Innerchr6:94075684..94103626hg19UCSC Ensembl
Innerchr6:94132405..94160347hg18UCSC Ensembl
Innerchr6:94132405..94160347hg17UCSC Ensembl
Cytoband6q16.1
Allele length
AssemblyAllele length
hg3827943
hg1927943
hg1827943
hg1727943
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv517329
Supporting Variants
Samples
Known GenesEPHA7
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv699707
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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