A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1029531



Internal ID19118750
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:111528670..111726303hg38UCSC Ensembl
Innerchr7:111168726..111366359hg19UCSC Ensembl
Innerchr7:110955962..111153595hg18UCSC Ensembl
Cytoband7q31.1
Allele length
AssemblyAllele length
hg38197634
hg19197634
hg18197634
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6586n100
Supporting Variantsnssv3751509
Samples
Known GenesDOCK4, IMMP2L
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1029531
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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