A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576174



Internal ID16363583
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81328349..81446410hg38UCSC Ensembl
Innerchr17:79302149..79413436hg19UCSC Ensembl
Innerchr17:76916744..77028031hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg38118062
hg19111288
hg18111288
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877110
Samples
Known GenesBAHCC1, LOC100130370, MIR4740, TMEM105
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv576174
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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