A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1031658



Internal ID18774192
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:127626828..127736721hg38UCSC Ensembl
Innerchr7:127266882..127376775hg19UCSC Ensembl
Innerchr7:127054118..127164011hg18UCSC Ensembl
Cytoband7q32.1
Allele length
AssemblyAllele length
hg38109894
hg19109894
hg18109894
Variant TypeCNV gain
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3662180
Samples
Known GenesSND1
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1031658
Frequency
Sample Size29084
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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