A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1033355



Internal ID18775889
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:158645675..159131365hg38UCSC Ensembl
Innerchr7:158438367..158924056hg19UCSC Ensembl
Innerchr7:158131128..158616817hg18UCSC Ensembl
Cytoband7q36.3
Allele length
AssemblyAllele length
hg38485691
hg19485690
hg18485690
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6772n100
Supporting Variantsnssv3757750
Samples
Known GenesESYT2, LINC00689, NCAPG2, VIPR2, WDR60
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1033355
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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