A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv515693



Internal ID15096300
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111088125..111103546hg38UCSC Ensembl
Innerchr7:110728181..110743602hg19UCSC Ensembl
Innerchr7:110515417..110530838hg18UCSC Ensembl
Innerchr7:110322132..110337553hg17UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg3815422
hg1915422
hg1815422
hg1715422
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv662032, nssv665621, nssv664556, nssv664439, nssv685131, nssv685523, nssv670724
Samples
Known GenesIMMP2L, LRRN3
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nsv515693
Frequency
Sample Size2026
Observed Gain7
Observed Loss0
Observed Complex0
Frequencyn/a


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