A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv682500



Internal ID15419152
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Innerchr6:151546595..151548510hg38UCSC Ensembl
Innerchr6:151867730..151869645hg19UCSC Ensembl
Innerchr6:151909423..151911338hg18UCSC Ensembl
Innerchr6:151959844..151961759hg17UCSC Ensembl
Cytoband6q25.1
Allele length
AssemblyAllele length
hg381916
hg191916
hg181916
hg171916
Variant TypeCNV loss
Copy Number
Allele StateHeterozygous
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv516304
Supporting Variants
Samples
Known GenesCCDC170
MethodSNP array
AnalysisSample-level CNVs
PlatformGPL6434
Comments
ReferenceShaikh_et_al_2009
Pubmed ID19592680
Accession Number(s)nssv682500
Frequency
Sample Size2026
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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