A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv2998776



Internal ID16945042
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr17:56592840..56598239hg38UCSC Ensembl
Outerchr17:54670201..54675600hg19UCSC Ensembl
Cytoband17q22
Allele length
AssemblyAllele length
hg385400
hg195400
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv952343
Supporting Variants
SamplesBILGI_BIOE
Known GenesNOG
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nssv2998776
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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