A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1026005



Internal ID18768537
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:72538245..72842566hg38UCSC Ensembl
Innerchr7:72003230..72313144hg19UCSC Ensembl
Innerchr7:71641166..71951080hg18UCSC Ensembl
Cytoband7q11.22
Allele length
AssemblyAllele length
hg38304322
hg19309915
hg18309915
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6459n100
Supporting Variantsnssv3655720
Samples
Known GenesMIR4650-1, MIR4650-2, SBDSP1, TYW1B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1026005
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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