A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034633



Internal ID18777167
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:10239..231133hg38UCSC Ensembl
Innerchr7:10239..231133hg19UCSC Ensembl
Innerchr7:52899..326216hg18UCSC Ensembl
Cytoband7p22.3
Allele length
AssemblyAllele length
hg38220895
hg19220895
hg18273318
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6213n100
Supporting Variantsnssv3654154, nssv3654153, nssv3654152, nssv3750952
Samples
Known GenesFAM20C, LOC100507642
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1034633
Frequency
Sample Size29084
Observed Gain4
Observed Loss0
Observed Complex0
Frequencyn/a


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