A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv3169972



Internal ID21314033
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr17:81402211..81421889hg38UCSC Ensembl
Outerchr17:81378673..81457300hg38UCSC Ensembl
Innerchr17:79376011..79395689hg19UCSC Ensembl
Outerchr17:79352473..79424326hg19UCSC Ensembl
Innerchr17:76990606..77010284hg18UCSC Ensembl
Outerchr17:76967068..77038921hg18UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg3878628
hg1971854
hg1871854
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv14249640
SamplesNGO_28
Known GenesBAHCC1, LOC100130370, MIR3186, MIR4740
MethodSNP array
Analysis
PlatformAffymetrix Genome-wide SNP array 6.0
Comments
ReferenceFu_et_al_2018
Pubmed ID29476164
Accession Number(s)nsv3169972
Frequency
Sample Size93
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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