A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980857



Internal ID18857558
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:122461184..122462084hg38UCSC Ensembl
Outerchr10:124220700..124221600hg19UCSC Ensembl
Cytoband10q26.13
Allele length
AssemblyAllele length
hg38901
hg19901
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118190
Supporting Variants
SamplesKWS1
Known GenesHTRA1
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980857
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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