A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3671171



Internal ID18622766
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144176847..144369842hg38UCSC Ensembl
Innerchr7:143873940..144066935hg19UCSC Ensembl
Innerchr7:143504873..143697868hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38192996
hg19192996
hg18192996
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1020823
Supporting Variants
Samples
Known GenesARHGEF34P, ARHGEF35, ARHGEF5, CTAGE4, CTAGE8, OR2A1, OR2A20P, OR2A42, OR2A7, OR2A9P, RNU6-57P
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nssv3671171
Frequency
Sample Size29084
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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