A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998804



Internal ID17291756
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:77723219..77728218hg38UCSC Ensembl
Outerchr17:75719301..75724300hg19UCSC Ensembl
Cytoband17q25.3
Allele length
AssemblyAllele length
hg385000
hg195000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952371
Supporting Variants
SamplesBILGI_BIOE
Known GenesLOC100132174
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998804
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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