A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029557



Internal ID19118776
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:143525976..143850167hg38UCSC Ensembl
Innerchr7:143223069..143547260hg19UCSC Ensembl
Innerchr7:142933191..143178193hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38324192
hg19324192
hg18245003
Variant TypeCNV gain+loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3670298, nssv3670295, nssv3670292, nssv3670297, nssv3670289, nssv3754735, nssv3670288, nssv3754732, nssv3670294, nssv3670293, nssv3670285, nssv3670296, nssv3670286, nssv3670291, nssv3754734, nssv3670287, nssv3754733, nssv3670299, nssv3670290
Samples
Known GenesCTAGE15, CTAGE6, FAM115C, LOC154761
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029557
Frequency
Sample Size11257
Observed Gain18
Observed Loss1
Observed Complex0
Frequencyn/a


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