A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv609002



Internal ID16049725
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr7:150970122..150980992hg38UCSC Ensembl
Innerchr7:150667210..150678080hg19UCSC Ensembl
Innerchr7:150298143..150309013hg18UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg3810871
hg1910871
hg1810871
Variant TypeCNV loss
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv1099499
Samples
Known GenesKCNH2
MethodSNP array
AnalysisIllumina SNP array copy number analysis
PlatformNot reported
Comments
ReferenceCooper_et_al_2011
Pubmed ID21841781
Accession Number(s)nsv609002
Frequency
Sample Size17421
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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