A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1015714



Internal ID18758248
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:144199147..144377836hg38UCSC Ensembl
Innerchr7:143896240..144074929hg19UCSC Ensembl
Innerchr7:143527173..143705862hg18UCSC Ensembl
Cytoband7q35
Allele length
AssemblyAllele length
hg38178690
hg19178690
hg18178690
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6727n100
Supporting Variantsnssv3672449, nssv3672448, nssv3756109, nssv3672450, nssv3672447, nssv3672446
Samples
Known GenesARHGEF34P, 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)nsv1015714
Frequency
Sample Size29084
Observed Gain0
Observed Loss6
Observed Complex0
Frequencyn/a


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