A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv747840



Internal ID15695110
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr10:51446996..51451622hg38UCSC Ensembl
Innerchr10:53206756..53211382hg19UCSC Ensembl
Innerchr10:52876762..52881388hg18UCSC Ensembl
Cytoband10q11.23
Allele length
AssemblyAllele length
hg384627
hg194627
hg184627
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv550861
Supporting Variants
Samples
Known GenesPRKG1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv747840
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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