A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1019601



Internal ID19108819
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144273205..144407069hg38UCSC Ensembl
Innerchr7:143970298..144104162hg19UCSC Ensembl
Innerchr7:143601231..143735095hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38133865
hg19133865
hg18133865
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6745n100
Supporting Variantsnssv3674186
Samples
Known GenesARHGEF34P, ARHGEF5, NOBOX, OR2A1, OR2A20P, OR2A42, 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)nsv1019601
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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