A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986856



Internal ID18858609
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr8:78687698..78687790hg38UCSC Ensembl
Outerchr8:79599933..79600025hg19UCSC Ensembl
Cytoband8q21.12
Allele length
AssemblyAllele length
hg3893
hg1993
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132155
Supporting Variants
SamplesKWS1
Known GenesZC2HC1A
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986856
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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