A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998737



Internal ID16945003
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:37989140..38250190hg38UCSC Ensembl
Outerchr17:36348701..36406200hg19UCSC Ensembl
Cytoband17q12
Allele length
AssemblyAllele length
hg38261051
hg1957500
Variant TypeCNV duplication
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv953891
Supporting Variants
SamplesBILGI_BIOE
Known GenesLOC440434
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998737
Frequency
Sample Size1
Observed Gain1
Observed Loss0
Observed Complex0
Frequencyn/a


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