A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv527014



Internal ID15454307
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:135149118..135206907hg38UCSC Ensembl
Innerchr7:134833870..134891659hg19UCSC Ensembl
Innerchr7:134484410..134542199hg18UCSC Ensembl
Innerchr7:134291125..134348914hg17UCSC Ensembl
Cytoband7q33
Allele length
AssemblyAllele length
hg3857790
hg1957790
hg1857790
hg1757790
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv703389
Samples
Known GenesC7orf49, TMEM140, WDR91
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv527014
Frequency
Sample Size2026
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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