A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1032918



Internal ID19122140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:56740039..56908389hg38UCSC Ensembl
Innerchr7:56807732..56976080hg19UCSC Ensembl
Innerchr7:56775226..56943574hg18UCSC Ensembl
Cytoband7p11.2
Allele length
AssemblyAllele length
hg38168351
hg19168349
hg18168349
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6364n100
Supporting Variantsnssv3661450, nssv3661453, nssv3661454, nssv3661451, nssv3661449, nssv3661447, nssv3661460, nssv3661448, nssv3661461, nssv3661452, nssv3661456, nssv3661455, nssv3661458, nssv3661457, nssv3661459
Samples
Known GenesLOC100130849
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1032918
Frequency
Sample Size11257
Observed Gain0
Observed Loss15
Observed Complex0
Frequencyn/a


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