A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3643375



Internal ID18594970
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:32925428..32999594hg38UCSC Ensembl
Innerchr7:32965040..33039206hg19UCSC Ensembl
Innerchr7:32931565..33005731hg18UCSC Ensembl
Cytoband7p14.3
Allele length
AssemblyAllele length
hg3874167
hg1974167
hg1874167
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1033096
Supporting Variants
Samples
Known GenesFKBP9, RP9P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3643375
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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