A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv951648



Internal ID16953835
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr7:150931413..151106413hg38UCSC Ensembl
Outerchr7:150628501..150803500hg19UCSC Ensembl
Cytoband7q36.1
Allele length
AssemblyAllele length
hg38175001
hg19175000
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv2998625
SamplesBILGI_BIOE
Known GenesABCB8, AGAP3, ASIC3, ATG9B, CDK5, FASTK, KCNH2, NOS3, SLC4A2, TMUB1
MethodSequencing
Analysis
PlatformIllumina HiSeq 2000
Comments
ReferenceDogan_et_al_2014
Pubmed ID24416366
Accession Number(s)nsv951648
Frequency
Sample Size1
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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