A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953826



Internal ID17302700
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:8158983..8164082hg38UCSC Ensembl
Outerchr17:8062301..8067400hg19UCSC Ensembl
Cytoband17p13.1
Allele length
AssemblyAllele length
hg385100
hg195100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv3000243
SamplesBILGI_BIOE
Known GenesVAMP2
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953826
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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