A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3968629



Internal ID18886280
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr18:80109416..80109716hg38UCSC Ensembl
Outerchr18:77867300..77867600hg19UCSC Ensembl
Cytoband18q23
Allele length
AssemblyAllele length
hg38301
hg19301
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1121958
Supporting Variants
SamplesKWS2
Known GenesADNP2
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3968629
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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