A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv3986779



Internal ID18875624
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:152408655..152408725hg38UCSC Ensembl
Outerchr7:152105740..152105810hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3871
hg1971
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv1132100
Supporting Variants
SamplesKWS1
Known GenesKMT2C
MethodSequencing
AnalysisHugeSeq
PlatformIllumina HiSeq 2000
Comments
ReferenceAlsmadi_et_al_2014
Pubmed ID24896259
Accession Number(s)nssv3986779
Frequency
Sample Size2
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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