A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv1152877



Internal ID15880017
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr3:174135994..174175248hg38UCSC Ensembl
Innerchr3:173853784..173893038hg19UCSC Ensembl
Innerchr3:175336478..175375732hg18UCSC Ensembl
Cytoband3q26.31
Allele length
AssemblyAllele length
hg3839255
hg1939255
hg1839255
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv592544
Supporting Variants
SamplesNINDS_142
Known GenesNLGN1
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nssv1152877
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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