A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv576173



Internal ID16363582
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81310814..81402198hg38UCSC Ensembl
Innerchr17:79284614..79375998hg19UCSC Ensembl
Innerchr17:76899209..76990593hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3891385
hg1991385
hg1891385
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv877109
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)nsv576173
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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