A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1017429



Internal ID19106646
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:56740039..56873818hg38UCSC Ensembl
Innerchr7:56807732..56941511hg19UCSC Ensembl
Innerchr7:56775226..56909005hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38133780
hg19133780
hg18133780
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6364n100
Supporting Variantsnssv3661443
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1017429
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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