A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3988869



Internal ID18890140
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:76495842..76501242hg38UCSC Ensembl
Outerchr10:78255600..78261000hg19UCSC Ensembl
Cytoband10q22.3
Allele length
AssemblyAllele length
hg385401
hg195401
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1111776
Supporting Variants
SamplesKWS2
Known GenesC10orf11
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3988869
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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