A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1020370



Internal ID18762905
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76443262..76801533hg38UCSC Ensembl
Innerchr7:76072579..76430850hg19UCSC Ensembl
Innerchr7:75910515..76268786hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38358272
hg19358272
hg18358272
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6472n100
Supporting Variantsnssv3656501
Samples
Known GenesDTX2, FDPSP2, LOC100133091, POMZP3, UPK3B
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1020370
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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