A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3980897



Internal ID19215849
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr12:9283804..9284304hg38UCSC Ensembl
Outerchr12:9436400..9436900hg19UCSC Ensembl
Cytoband12p13.31
Allele length
AssemblyAllele length
hg38501
hg19501
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1118226
Supporting Variants
SamplesKWS1
Known GenesLOC642846
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3980897
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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