A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1025057



Internal ID19114275
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:76443262..76936433hg38UCSC Ensembl
Innerchr7:76072579..76565750hg19UCSC Ensembl
Innerchr7:75910515..76403686hg18UCSC Ensembl
Cytoband7q11.23
Allele length
AssemblyAllele length
hg38493172
hg19493172
hg18493172
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6473n100
Supporting Variantsnssv3656504, nssv3656503
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)nsv1025057
Frequency
Sample Size11257
Observed Gain2
Observed Loss0
Observed Complex0
Frequencyn/a


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