A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3970318



Internal ID18900464
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr10:32808602..32808661hg38UCSC Ensembl
Outerchr10:33097530..33097589hg19UCSC Ensembl
Cytoband10p11.22
Allele length
AssemblyAllele length
hg3860
hg1960
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1133984
Supporting Variants
SamplesKWS2
Known GenesCCDC7
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3970318
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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