A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1034654



Internal ID19123875
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:124951379..125033319hg38UCSC Ensembl
Innerchr7:124591433..124673373hg19UCSC Ensembl
Innerchr7:124378669..124460609hg18UCSC Ensembl
Cytoband7q31.33
Allele length
AssemblyAllele length
hg3881941
hg1981941
hg1881941
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variantsdgv6607n100
Supporting Variantsnssv3751534, nssv3662143
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)nsv1034654
Frequency
Sample Size11257
Observed Gain0
Observed Loss2
Observed Complex0
Frequencyn/a


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