A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1030170



Internal ID19119389
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:88507567..88624949hg38UCSC Ensembl
Innerchr7:88136882..88254263hg19UCSC Ensembl
Innerchr7:87974818..88092199hg18UCSC Ensembl
Cytoband7q21.12
Allele length
AssemblyAllele length
hg38117383
hg19117382
hg18117382
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6524n100
Supporting Variantsnssv3655196, nssv3655195
Samples
Known Genes
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1030170
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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