A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1022937



Internal ID18765471
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76443262..76972256hg38UCSC Ensembl
Innerchr7:76072579..76601573hg19UCSC Ensembl
Innerchr7:75910515..76439509hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38528995
hg19528995
hg18528995
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6474n100
Supporting Variantsnssv3755332, nssv3656506
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)nsv1022937
Frequency
Sample Size29084
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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