A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv957657



Internal ID17306530
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:130838517..130840514hg38UCSC Ensembl
Outerchr8:131850763..131852760hg19UCSC Ensembl
Cytoband8q24.22
Allele length
AssemblyAllele length
hg381998
hg191998
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3001083
SamplesBILGI_BIOE
Known GenesADCY8
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv957657
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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