A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv1018125



Internal ID19107342
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:26705455..26750195hg38UCSC Ensembl
Innerchr7:26745074..26789814hg19UCSC Ensembl
Innerchr7:26711599..26756339hg18UCSC Ensembl
Cytoband7p15.2
Allele length
AssemblyAllele length
hg3844741
hg1944741
hg1844741
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3643322
Samples
Known GenesSKAP2
MethodSNP array
AnalysisAffymetrix SNP array copy number analysis
PlatformAffymetrix SNP Array 6.0
Comments
ReferenceCoe_et_al_2014
Pubmed ID25217958
Accession Number(s)nsv1018125
Frequency
Sample Size11257
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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