A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv953895



Internal ID16956082
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:39730748..39746847hg38UCSC Ensembl
Outerchr17:37887001..37903100hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg3816100
hg1916100
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998741
SamplesBILGI_BIOE
Known GenesGRB7
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv953895
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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